In territorial Kansas’ first election, some 5,000 so-called “Border Ruffians” invade the territory from western Missouri and force the election of a pro-slavery legislature. Although the number of votes cast exceeded the number of eligible voters in the territory, Kansas Governor …read more

1533 – Henry VIII divorced his first wife, Catherine of Aragon.

1814 – The allied European nations against Napoleon marched into Paris.

1822 – Florida became a U.S. territory.

1842 – Dr. Crawford W. Long performed the first operation while his patient was anesthetized by ether.

1855 – About 5,000 “Border Ruffians” from western Missouri invaded the territory of Kansas and forced the election of a pro-slavery legislature. It was the first election in Kansas.

1856 – A peace treaty was signed between England and Russia. (Treaty of Paris)

1858 – Hyman L. Lipman of Philadelphia patented the pencil.

1867 – The U.S. purchased Alaska from Russia for $7.2 million dollars.

1870 – The 15th amendment, guaranteeing the right to vote regardless of race, was passed by the U.S. Congress.

1870 – Texas was readmitted to the Union.

1903 – Revolutionary activity in the Dominican Republic brought U.S. troops to Santo Domingo to protect American interests.

1905 – U.S. President Theodore Roosevelt was chosen to mediate in the Russo-Japanese peace talks.

1909 – The Queensboro bridge in New York opened linking Manhattan and Queens. It was the first double decker bridge.

1909 – In Oklahoma, Seminole Indians revolted against meager pay for government jobs.

1916 – Pancho Villa killed 172 at the Guerrero garrison in Mexico.

1936 – Britain announced a naval construction program of 38 warships.

1939 – The comic book “Detective Comics #27” appeared on newstands. This comic introduced Batman.

1940 – The Japanese set up a puppet government called Manchuko in Nanking, China.

1941 – The German Afrika Korps under General Erwin Rommel began its first offensive against British forces in Libya.

1944 – The U.S. fleet attacked Palau, near the Philippines.

1945 – The U.S.S.R. invaded Austria during World War II.

1946 – The Allies seized 1,000 Nazis attempting to revive the Nazi party in Frankfurt.

1947 – Lord Mountbatten arrived in India as the new Viceroy.

1950 – The invention of the phototransistor was announced.

1950 – U.S. President Truman denounced Senator Joe McCarthy as a saboteur of U.S. foreign policy.

1957 – Tunisia and Morocco signed a friendship treaty in Rabat.

1958 – The Alvin Ailey American Dance Theater gave its initial performance.

1964 – “Jeopardy” debuted on NBC-TV.

1964 – John Glenn withdrew from the Ohio race for U.S. Senate because of injuries suffered in a fall.

1970 – “Applause” opened on Broadway.

1970 – “Another World – Somerset” debuted on NBC-TV.

1972 – The British government assumed direct rule over Northern Ireland.

1972 – The Eastertide Offensive began when North Vietnamese troops crossed into the Demilitarized Zone (DMZ) in the northern portion of South Vietnam.

1975 – As the North Vietnamese forces moved toward Saigon South Vietnamese soldiers mob rescue jets in desperation.

1981 – U.S. President Ronald Reagan was shot and wounded in Washington, DC, by John W. Hinckley Jr. Two police officers and Press Secretary James Brady were also wounded.

1982 – The space shuttle Columbia completed its third and its longest test flight after 8 days in space.

1984 – The U.S. ended its participation in the multinational peace force in Lebanon.

1987 – Vincent Van Gogh’s “Sunflowers” was bought for $39.85 million.

1993 – In Sarajevo, two Serb militiamen were sentenced to death for war crimes committed in Bosnia.

1993 – In the Peanuts comic strip, Charlie Brown hit his first home run.

1994 – Serbs and Croats signed a cease-fire to end their war in Croatia while Bosnian Muslims and Serbs continued to fight each other.

1998 – Rolls-Royce was purchased by BMW in a $570 million deal.

2002 – An unmanned U.S. spy plan crashed at sea in the Southern Philippines.

2002 – Suspected Islamic militants set off several grenades at a temple in Indian-controlled Kashmir. Four civilians, four policemen and two attackers were killed and 20 people were injured.

2009 – The Port Authority of New York and New Jersey confirmed that the new World Trade Center building would be officially known by its legal name of “One World Trade Center.”

on-this-day.com

** 008-2022, Boyd Specialties, LLC Recalls Jerky Products Due to Possible Listeria Contamination (Mar 4, 2022}

** 63-count and 75-count Bottles of AIRBORNE^® Gummies

The health and safety of consumers is our top priority. Therefore, Reckitt  is voluntarily recalling certain 63-count and 75-count bottles of Airborne® Gummies in Assorted Fruit, Orange, and Blueberry Pomegranate flavors that were distributed in the United States between May 2020 and February 2022. Pressure build up in the bottle can cause the cap and underlying seal to pop off with force when opened for the first time, posing an injury hazard. This product recall is being conducted in cooperation with the U.S. Consumer Product Safety Commission.

If you have unopened bottles of 63-count and 75-count Bottles of AIRBORNE® BRAND GUMMIES, PLEASE DO NOT OPEN the product. Use the Lot code search tool to identify whether your product is included in this recall OR refer to the charts here

Consumers with unopened bottles should contact Reckitt to return the unopened bottles to receive a full refund. Postage-paid labeling will be provided for the item to be returned. Please contact our Recall Hotline at 1-888-266-8003 (Monday – Friday, 8 a.m. to 5 p.m. Eastern Time).

Important: Bottles that have already been opened are not subject to this recall as they would have released any pressure build up and do not present an injury hazard. The Gummy product inside the bottle is unaffected by the pressure build up and remains safe to consume as directed on the label.

Please note – Our Elderberry and Honey Lemon varieties are not impacted.

Q&A

 Why are some lots of Airborne Gummies being recalled? What is the hazard?

Reckitt has received reports that pressure build up in the bottle can cause the cap and underlying seal to pop off with force when opened for the first time, posing an injury hazard. Bottles that have already been opened are not subject to this recall as they would have released any pressure build up and do not present an injury hazard.

I already opened a bottle that is covered by the recall. Are the gummies safe to consume?

The Gummy product inside the bottle is unaffected by this pressure build up and remains safe to consume as directed on the label. 

How can I identify if I have a bottle subject to the recall?

Affected bottles can be identified by locating the UPC / SKU on the outside of the bottle, and the lot number and expiration date on the bottom of the plastic bottle. (Scroll further down the page to see photos.)

*Please note: For Airborne Gummies bundle packs (2 x 63-count bottles), the UPC may not be as easily visible, so please use the lot code and expiration on the bottom of the bottle to identify product with the affected packaging.

What should I do if I have the recalled bottle?

If you have unopened bottles of 63-count and 75-count Bottles of AIRBORNE® BRAND GUMMIES that are part of this recall, PLEASE DO NOT OPEN the product.

Consumers with unopened bottles should contact Reckitt to return the unopened bottles to receive a full refund. Postage-paid labeling will be provided for the item to be returned. Please contact our Recall Hotline at 1-888-266-8003 (Monday – Friday, 8 a.m. to 5 p.m. Eastern Time).

Bottles that have already been opened are not subject to this recall as they would have released any pressure build up and do not present an injury hazard.

Can I get a refund or replacement for unopened product in my possession that is part of this recall?

Yes. Please contact our Recall Hotline at 1-888-266-8003 (Monday – Friday, 8 a.m. to 5 p.m. Eastern Time) to return the unopened bottles to receive a full refund. Postage-paid labeling will be provided for the item to be returned. 

Which product lots have the affected packaging and are part of this recall?

Only the lots listed below are part of this recall.

Consumers can continue to use other Airborne products and Reckitt supplements with confidence.

63CT PRODUCT LOTS AFFECTED BY RECALL: 

12-digit UPC /SKU	Description	Lot Code	Expiration
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC1270G	11/30/2021
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC1400A	11/30/2021
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC1400B	11/30/2021
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC1900H	3/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC2180C	4/30/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC2320A	4/30/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3080A	7/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3300A	7/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3300B	7/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3080E	7/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3440B	8/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3440C	8/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3440J	8/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC3440K	8/31/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC0301H	9/30/2022
6-47865-96299-1	AIRBORNE® Gummies – Assorted Fruit 63 ct.	AC0301A	9/30/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC1350B	1/31/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC1690B	2/28/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC1690D	2/28/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC2030A	3/31/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC1690C	2/28/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC2570A	5/31/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC3140D	6/30/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC2850D	6/30/2022
6-47865-96339-4	AIRBORNE® Gummies – Orange 63 ct.	AC2850E	6/30/2022
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC1620B	12/31/2021
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC1330D	11/30/2021
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC1620A	12/31/2021
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC1790C	2/28/2022
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC0661B	11/30/2022
6-47865-99557-9	AIRBORNE® Gummies – Kids 63 ct.	AC0661C	11/30/2022
6-47865-99601-9	AIRBORNE® Gummies – Blueberry Pomegranate 63 ct.	AC1041A	12/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC1270G	11/30/2021
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC1400A	11/30/2021
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC1400B	11/30/2021
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC1900H	3/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC2180C	4/30/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit (2×63) ct.	AC2320A	4/30/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3080A	7/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3300A	7/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3300B	7/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3080E	7/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3440B	8/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3440C	8/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3440J	8/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC3440K	8/31/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC0301H	9/30/2022
6-47865-99564-7	AIRBORNE® Gummies – Assorted Fruit Bundle Pack (2×63) ct.	AC0301A	9/30/2022

 

 75CT PRODUCT LOTS AFFECTED BY RECALL: 

12-digit UPC /SKU	Description	Lot Code	Expiration
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1140G	10/31/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1140H	10/31/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1140I	10/31/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1270D	11/30/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1640A	12/31/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1640B	12/31/2021
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1780G	2/28/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2060F	3/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2060G	3/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2180A	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2180B	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2180D	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2180E	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2320B	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2320C	4/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2770G	6/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2770J	6/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2560F	5/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC3080B	7/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC3080C	7/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC3080D	7/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC2560J	5/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC3440A	8/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC0441B	10/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC0441D	10/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC0301I	9/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC0691B	11/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC0691C	11/30/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1051A	12/31/2022
6-47865-18574-1	AIRBORNE® Gummies – Assorted Fruit 75 ct.	AC1580E	2/2/2022
6-47865-90530-1	AIRBORNE® Gummies Kids – Assorted Fruit 75 ct.	AC2040D	3/31/2022
6-47865-90530-1	AIRBORNE® Gummies Kids – Assorted Fruit 75 ct.	AC3020B	6/30/2022
6-47865-90530-1	AIRBORNE® Gummies Kids – Assorted Fruit 75 ct.	AC0661D	11/30/2022

**  Adamis Pharmaceuticals CorporationExternal Link Disclaimer (Nasdaq: ADMP) is voluntarily recalling certain lots of SYMJEPI (epinephrine) Injection 0.15 mg (0.15 mg/0.3 mL) and 0.3 mg (0.3 mg/0.3 mL) Pre-Filled Single-Dose Syringes to the consumer level. The batches in the table below are being recalled due to the potential clogging of the needle preventing the dispensing of epinephrine. US WorldMeds (USWM) exclusively markets and distributes SYMJEPI in the United States, under license from Adamis, the NDA holder. USWM will handle the entire recall process for Adamis, with Adamis oversight. SYMJEPI is manufactured and tested for Adamis by Catalent Belgium S.A.

Risk Statement:

If a person is experiencing an allergic reaction and/or anaphylaxis and is unable to access life-saving epinephrine due to the syringe malfunction, it can lead to life threatening consequences including death. Although not confirmed to be related to the recall, there have been two different customer complaints on three syringes, regarding difficulty in dispensing the product, to date. However, neither US WorldMeds nor Adamis Pharmaceuticals has received, or is aware of, any adverse events related to this recall.

The recall encompasses all of the following batches, within expiry:

Product	Strength	NDC	Lot	Expiration
SYMJEPI (epinephrine) Injection	0.15 mg/0.3 mL	78670-131-02	21101Y	11/30/2022
0.3 mg/0.3 mL	78670-130-02	21041W	8/31/2022
21081W	11/30/2022
21102W	2/28/2023

SYMJEPI is indicated in the emergency treatment of allergic reactions (Type I) including anaphylaxis to stinging insects (e.g., order Hymenoptera, which include bees, wasps, hornets, yellow jackets, and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.

The products are packaged in 2-count Pre-Filled Single-Dose Syringes per carton and were distributed nationwide in the USA and directly to customers and/or medical facilities. The products can be identified by the label containing the US WorldMeds name and logo pictured on the cartons below.

US WorldMeds is notifying its customers by email, FDA alerts, and direct outreach. Consumers and institutions that have products that are subject to this recall should stop using the products immediately and may either return or discard the recalled lots. Consumers with questions regarding this recall can call (888) 900-8796 or e-mail questions at medinfo@usworldmeds.com Monday-Friday from 8:00 am to 4:00 pm ET.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online
• Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

** Farm Fresh Produce LLC of Vernon, CA, is recalling all of the 14.11 ounce packages of “TWA AGRICULTURE MIXED MUSHROOMS” because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled ” TWA AGRICULTURE MIXED MUSHROOMS ” were distributed nationwide in retail store.

The product comes in a 14.11 ounce, clear plastic package marked with UPC6957937481850.

No illnesses have been reported to date in connection with this problem.

The potential for contamination was noted after routine testing by the California Department of Public Health (CDPH) revealed the presence of Listeria monocytogenes in 14.11 ounce packages of ” TWA AGRICULTURE MIXED MUSHROOMS.”

The production of the product has been suspended while FDA and the company continue to investigate the source of the problem.

Consumers who have purchased 14.11  ounce packages of ” TWA AGRICULTURE MIXED MUSHROOMS.”” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-323-583-1128 ( Monday – Friday 6:00am – 1:30pm).

** Princeton, NJ, Sandoz Inc. (“Sandoz”) is initiating a voluntary recall of 13 lots (listed below) of oral Orphenadrine Citrate 100 mg Extended Release (ER) Tablets to the consumer level. The presence of a nitrosamine (N-methyl-N-nitroso-2-[(2-methylphenyl)phenylmethoxy]ethanamine (NMOA or Nitroso-Orphenadrine)) impurity, which has the potential to be above the U.S. Food and Drug Administration (FDA)’s Acceptable Daily Intake (ADI) limit of 26.5 ng/day, was detected in the lots during recent testing. These 13 lots of Orphenadrine Citrate ER Tablets were shipped to customers from August 2019 to April 2021.

Nitrosamines are substances with carcinogenic potency (substances that could cause cancer) when present above the allowable exposure limits. While the use of product belonging to the recalled lots may represent a risk to patients, to date, Sandoz has not received any reports of adverse events related to the presence of a nitrosamine impurity in the lot.

Orphenadrine Citrate ER Tablets are used as an adjunct to rest, physical therapy and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions. The product is packaged in 100-count and 1000-count bottles and was distributed nationwide in the USA to wholesalers and distributors.

Product Name	NDC Number	Lot Number	Expiration Date	Date of Manufacture
Orphenadrine Citrate ER Tablets	0185-0022-01	JX6411	05/2022	5/24/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	JX6413	05/2022	5/24/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KC0723	08/2022	8/21/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KC3303	08/2022	8/21/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KE4348	11/2022	11/6/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KE7169	11/2022	11/6/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KE4349	11/2022	11/6/2019
Orphenadrine Citrate ER Tablets	0185-0022-01	KL3199	03/2023	3/3/2020
Orphenadrine Citrate ER Tablets	0185-0022-01	KM0072	03/2023	3/3/2020
Orphenadrine Citrate ER Tablets	0185-0022-10	KS3939+	03/2023	3/3/2020
Orphenadrine Citrate ER Tablets	0185-0022-01	LA7704	10/2023	10/6/2020
Orphenadrine Citrate ER Tablets	0185-0022-01	LA7703	10/2023	10/6/2020
Orphenadrine Citrate ER Tablets	0185-0022-01	LA9243	11/2023	11/18/2020

+ 1,000-count bottle

This recall of Orphenadrine Citrate ER Tablets is specific to the lots listed above and does not apply to any other strengths of Sandoz Orphenadrine Citrate ER Tablets nor to other lot numbers of the product. Any product returned that is not associated with this recall will be destroyed, and no credit will be issued.

Sandoz is notifying its wholesalers and distributors by mail and is arranging for the return of all recalled product. Wholesalers and distributors that have Orphenadrine Citrate ER Tablets subject to this recall should immediately stop distribution of the recalled product and quarantine and return all recalled product in their inventory.

Consumers who have Orphenadrine Citrate ER Tablets being recalled should stop taking the recalled product and immediately consult with their physician to obtain another prescription. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Retailers and consumers should contact Sedgwick directly by phone at 844-491-7869 or email at sandoz4887@sedgwick.com to return the recalled product. Representatives are available Monday – Friday, 8:00 am – 5:00 pm ET.

** WiseTrade Corporation of Irvine, CA is recalling all its cases of its 200g/7.05oz packages of ENOKI MUSHROOM (Product of Korea) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled Enoki Mushroom product was distributed in CA to produce distributors or wholesalers for further distribution to retail stores.

The Enoki Mushroom comes in a 200g/7.05oz clear plastic package with the following description “Global Fresh Marketing Enoki Mushrooms” in the front and back Wisetrade Coporation Irvine, CA 92618. 

The UPC is 809728-95012 on the back side of the package.

There is no lot code or dates on a package.

No illnesses have been reported to date in connection with this problem. The distribution of the product has been suspended.

The potential for contamination was discovered after a retail sample collected and analyzed by California Department of Public Health (CDPH) and revealed the presence of Listeria monocytogenes in 7.05 oz. package of Enoki mushroom.

This recall is being made with the knowledge of the U.S. Food and Drug Administration and CDPH.

Consumers who have purchased 200g packages of Enoki are urged to return them to the place of purchase for a full refund. Consumers with question may contact the company at 949-264-2268 Monday – Friday 7:00am – 3:00pm PST.

** 3/24/2022 – Lawrence, KS, Plastikon Healthcare, LLC is voluntarily recalling three (3) lots of Milk of Magnesia 2400 mg/30 mL Oral Suspension, one (1) lot of Acetaminophen 650mg/ 20.3mL, and six (6) lots of Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL to the hospital, clinic and patient level.  The products are being recalled due to microbial contamination and failure to properly investigate failed microbial testing.

Risk Statement: This product potentially could result in illness due to intestinal distress, such as diarrhea or abdominal pain.  Individuals with a compromised immune system have a higher probability of developing a wide-spread, potentially life-threatening infection when ingesting or otherwise orally exposed to products contaminated by micro-organisms. To date, Plastikon has not received any customer complaints related to microbial concerns or reports of adverse events related to this recall.

Product indication, lot numbers, expiration dates and NDC information are listed in the table below. The product is packaged for institutional use and is sold to clinics and hospitals nationwide in single use cups with a foil lid.  The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 5/1/2020 and 6/28/2021, who shipped to hospitals, nursing homes, and clinics nationwide.  The products are private labeled for Major Pharmaceuticals.

Product Name	Milk of Magnesia 2400 mg/30 mL Oral Suspension	Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL	Acetaminophen 650mg/ 20.3mL
Indications for use	Milk of Magnesia 2400 mg/ 30 mL is indicated for the occasional relief of constipation (irregularity) in adults and children 12 years and older or for children under 12 as recommended by a doctor.	Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL is indicated for relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating commonly referred to as gas.	Acetaminophen 650mg/ 20.3mL indicated for temporarily relief of minor aches and pains due to, minor pain of arthritis, muscular aches, backache, premenstrual and menstrual cramps, the common cold, headache, toothache, and temporarily reduction of fever.
Lot/exp.	20024A/Mar 2022 20025A/Mar 2022 20041A/May 2022	20042A/May 2022 20043A/May 2022 20045A/May 2022 20046A/May 2022 20047A/May 2022 21067A/Jun 2023	20040A/May 2022
NDC	0904-6846-73	0904-6838-73	0904-6820-76
Type of Packaging	Carton containing 100 single dose cups (10 trays x 10 cups)	Carton containing 100 single dose cups (10 trays x 10 cups)	Carton containing 100 single dose cups (10 trays x 10 cups)

Plastikon Healthcare places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process.  Plastikon Healthcare has notified its direct customers via a recall letter to arrange for return of any recalled product.  Anyone with an existing inventory of the lots which are being recalled should stop use and distribution, and quarantine immediately.  Return all quarantined product to the place of purchase. For clinics, hospitals, or healthcare providers that have dispensed product to patients, please notify patients regarding the recall.

Consumers with questions regarding this recall can contact Plastikon by phone at 785-330-7109 or email address (sdixon@plastikon.com) Monday through Friday from 9 am to 4 pm CST.  Patients are advised to contact their doctor or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

** Continental Mills has issued a recall of Kroger Buttermilk Pancake & Waffle Mix, due to a potential foreign material contamination. Fragments from a cable used to clear the processing line were discovered in a limited amount of product.

The Kroger Buttermilk Pancake & Waffle Mix is packaged in a box, net wt. 2 lbs., UPC 01111088219. The affected product has the lot codes KX2063 and KX2064, Best By Date of 09/01/2023 and 09/02/2023.

Product was distributed to Kroger stores in the following states: AL, AR, FL, GA, IL, IN, KY, LA, MI, MO, MS, OH, SC, TN, TX, VA, WV.

No contaminated product has been reported by consumers to date. No injuries have been reported to date.

If you have recently purchased any of the products noted above, please dispose of the product. For more information about the recall or information to receive a refund, please call the Recall Phone Hotline at 1-800-578-7832 Monday – Friday 7 am to 4 pm PT.

** CINCINNATI, Ohio, March 11, 2022 – Kao USA Inc. is asking consumers to check their Jergens® Ultra Healing Moisturizer 3 oz and 10 oz products to determine if it is part of a voluntary recall of the product.

Select units of Jergens® Ultra Healing Moisturizer could show the presence of Pluralibacter gergoviae, a bacterium which typically poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems may be more susceptible to infections. Kao USA is urging consumers to discontinue use of the recalled lotion specified below as a precautionary measure.

Further investigation to determine the scope of the issue is still ongoing. However, Kao USA Inc. promptly took the precautionary step of issuing a voluntary recall of the affected product by removing the product in question from warehouses, working with retailers to ensure the product is removed from store shelves, and proactively notifying consumers.

Kao USA cares about our consumers’ safety. We are committed to manufacturing products that not only meet, but exceed, the highest industry standards.

The amount of recalled product is limited to two sizes offered for Jergens® Ultra Healing Moisturizer. Only specific lots of the 3 oz and 10 oz sizes are affected.

IDENTIFYING THE AFFECTED PRODUCTS

• Jergens® Ultra Healing Moisturizer, manufactured between October 1, 2021 and October 18, 2021, could be impacted.
• The affected lot codes for the 3 oz size (UPC 019100109971 for single bottles and 019100267114 for pack of 3) can be found on the back of the bottle printed in black ink and begin with the prefix “ZU”:

ZU712851	ZU712871
ZU712911	ZU722881
ZU712861	ZU712881
ZU722851

• The affected lot codes for the 10 oz size (UPC 019100109988) can be found on the bottom of the bottle printed in black ink and begin with the prefix “ZU”:

ZU722741	ZU722781
ZU732791	ZU732811
ZU722771	ZU732781
ZU732801	ZU732821

Kao USA Inc. will inform regulatory authorities of the issue and we are working with our partners on improved cleaning and sanitization practices so that similar issues can be prevented in the future.

Anyone who has product from a recalled lot should call the Kao USA Inc. Consumer Care Center for a free product coupon at the following number: 1.800.742.8798 or send an email to: consumer@kao.com. (Hours of operation: Monday – Friday, 9AM – 5PM US ET) A postage paid label and plastic bag will be sent to consumers via mail to easily return the product.

** Continental Mills Recalls Walmart Great Value Buttermilk Pancake & Waffle Mix Due to Possible Foreign Material Contamination

Continental Mills has issued a recall for a single lot of Great Value Buttermilk Pancake & Waffle Mix, UPC 078742370828, Lot code KX2063, Best By Date of 09/01/2023, due to a potential foreign material contamination. Fragments from a cable used to clear the processing line were discovered in a limited amount of product.

The affected product was distributed nationwide where consumers purchased product through retail Walmart stores.

No contaminated product has been reported by consumers to date. No injuries have been reported to date. If you have recently purchased any of the products noted above, please dispose of the product or please return the product to your store for a replacement or refund. For more information or to receive a refund, please call the Recall Phone Hotline at 1-800-578-7832 Monday Friday 7 am to 4 pm PT.

**  Adamis Pharmaceuticals CorporationExternal Link Disclaimer (Nasdaq: ADMP) is voluntarily recalling certain lots of SYMJEPI (epinephrine) Injection 0.15 mg (0.15 mg/0.3 mL) and 0.3 mg (0.3 mg/0.3 mL) Pre-Filled Single-Dose Syringes to the consumer level. The batches in the table below are being recalled due to the potential clogging of the needle preventing the dispensing of epinephrine. US WorldMeds (USWM) exclusively markets and distributes SYMJEPI in the United States, under license from Adamis, the NDA holder. USWM will handle the entire recall process for Adamis, with Adamis oversight. SYMJEPI is manufactured and tested for Adamis by Catalent Belgium S.A.

Risk Statement:

If a person is experiencing an allergic reaction and/or anaphylaxis and is unable to access life-saving epinephrine due to the syringe malfunction, it can lead to life threatening consequences including death. Although not confirmed to be related to the recall, there have been two different customer complaints on three syringes, regarding difficulty in dispensing the product, to date. However, neither US WorldMeds nor Adamis Pharmaceuticals has received, or is aware of, any adverse events related to this recall.

The recall encompasses all of the following batches, within expiry:

Product	Strength	NDC	Lot	Expiration
SYMJEPI (epinephrine) Injection	0.15 mg/0.3 mL	78670-131-02	21101Y	11/30/2022
0.3 mg/0.3 mL	78670-130-02	21041W	8/31/2022
21081W	11/30/2022
21102W	2/28/2023

SYMJEPI is indicated in the emergency treatment of allergic reactions (Type I) including anaphylaxis to stinging insects (e.g., order Hymenoptera, which include bees, wasps, hornets, yellow jackets, and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.

The products are packaged in 2-count Pre-Filled Single-Dose Syringes per carton and were distributed nationwide in the USA and directly to customers and/or medical facilities. The products can be identified by the label containing the US WorldMeds name and logo pictured on the cartons below.

US WorldMeds is notifying its customers by email, FDA alerts, and direct outreach. Consumers and institutions that have products that are subject to this recall should stop using the products immediately and may either return or discard the recalled lots. Consumers with questions regarding this recall can call (888) 900-8796 or e-mail questions at medinfo@usworldmeds.com Monday-Friday from 8:00 am to 4:00 pm ET.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online
• Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

** The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the salad dressing component of ready-to-eat (RTE) salad products containing meat and poultry may contain egg, milk, peanut or wheat, known allergens, which are not declared on the product labels. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed.

The salad products were produced March 8, 2022 to March 17, 2022. The following products are subject to the public health alert: [view labels (PDF only)]

• 12-oz. plastic container of “Charlie’s DELIVERED FRESH DAILY SOUTHWEST SALAD” with best by dates 3/15/22 through 3/24/22, that may include Thai-style salad dressing, which contains undeclared peanut and wheat.
• 12-oz. plastic container of “Charlie’s DELIVERED FRESH DAILY CHICKEN BLT SALAD” with best by dates 3/15/22 through 3/24/22, that may include Thai-style salad dressing, which contains undeclared peanut.
• 11-oz. plastic container of “Signature Café THAI Style Salad with White Meat Chicken” with best by dates 3/15/22 through 3/24/22, that may include BBQ Ranch salad dressing, which contains undeclared egg and milk.

The products bear establishment number “P-38458” inside the USDA mark of inspection. These items were shipped to retail and food service locations in Alaska.

The problem was discovered when the producing establishment notified FSIS that it received a consumer complaint that incorrect salad dressing was included in the salad packaging.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

FSIS has verified the affect products are no longer available for sale but is concerned that some products may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Consumers and members of the media with questions about the public health alert can contact Oliver Evans, Division President, Charlie’s Produce, at 907-258-1412 or anchoragefoodsafety@charliesproduce.com.

** ACON Laboratories Issues a Recall of Non-EUA Authorized Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) Tests From the U.S. Market

SAN DIEGO, CA, January 9, 2022 ACON Laboratories, Inc. (ACON Laboratories), the legal manufacturer of the Flowflex COVID-19 Antigen Home Test (FDA Emergency Use Authorization EUA210494), has identified the U.S. distribution of unauthorized, adulterated and misbranded counterfeit product having the trade name FlowflexSARS-CoV-2 Antigen Rapid Test (Self-Testing). ACON Laboratories is not importing the Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) into the U.S. as it is only authorized for sale in Europe and other markets, under the CE mark. This press release serves as public announcement that this CE marked product is being recalled from the U.S. market. The FlowflexSARS-CoV-2 Antigen Rapid Test (Self-Testing) cannot be legally imported, distributed, or used in the U.S. market as it has not been approved, cleared, or authorized by the FDA. The FlowflexCOVID-19 Antigen Home Test cannot be legally imported, distributed, or used in the European market as it is not CE marked.

** Jan Fruits Inc. of VERNON, CA is recalling all its cases of its 200g/7.05oz packages of ENOKI MUSHROOM (Product of Taiwan) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever,severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled Enoki Mushroom product was distributed in CA to produce distributors or wholesalers for further distribution to retail stores.

The Enoki Mushroom comes in a 200g/7.05oz clear plastic package with the following description “Taiwan Best Quality Enoki Natural Mushroom***Manufacturer: Changhua County Mushrooms Production Cooperative” in English. There is a green lettered “Premium” Printed with two QR scan codes and UPC 8 51084 00835 8 on the back side of a package There is a Lot Code #3322 outside of box.

No illnesses have been reported to date in connection with this problem. The distribution of the product has been suspended.

The potential for contamination was discovered after a retail sample collected and analyzed by California Department of Public Health (CDPH) and revealed the presence of Listeria monocytogenes in 7.05 oz. package of Enoki mushroom.

This recall is being made with the knowledge of the U.S. Food and Drug Administration and CDPH.

Consumers who have purchased 200g packages of Enoki are urged to return them to the place of purchase for a full refund. Consumers with question may contact the company at 323-923-2879 Ext. 3. Monday – Friday 7:00am – 3:00pm PST.

** T Fresh Company of City of Industry, CA is recalling its 5.25oz (150g) enoki mushrooms, Lot #6021053 grown in China & 7.5oz (200g) Lot # 6021052 grown in China, because it has the potential to be contaminated withlisteria monocytogenes, a bacterium which can cause life-threatening illness.

Symptoms oflisteriamay include fever, muscle aches, severe headache, nausea, vomiting, stiff neck, confusion, loss of balance, and convulsions. People experiencing these problems should seek immediate medical attention. This bacteria can be completely destroyed and the risk of infection can be eliminated by thoroughly cooking foods at temperatures of 165F (73.8C). Lot #6021053 was distributed from California and Texas to retail stores through produce distributors, while traces of the bacterium were discovered by CDPH sampling. Product is packaged in a pink and transparent plastic packaging, with the Yes Logo for the 150g(5.25oz) & Light Blue & transparent plastic packaging, with ” Yes” Logo for the 200g(7.5oz). Enoki mushrooms are white, stringy with small caps. The weight of the product is 5.25 oz (150g) & 7.5 oz (200g). The UPC barcode numbers are 825382736718 (150g), with no other codes & 825382736947 (200g), with no other codes.

** Ohio, March 11, 2022 – Kao USA Inc. is asking consumers to check their Jergens® Ultra Healing Moisturizer 3 oz and 10 oz products to determine if it is part of a voluntary recall of the product.

Select units of Jergens® Ultra Healing Moisturizer could show the presence of Pluralibacter gergoviae, a bacterium which typically poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems may be more susceptible to infections. Kao USA is urging consumers to discontinue use of the recalled lotion specified below as a precautionary measure.

Further investigation to determine the scope of the issue is still ongoing. However, Kao USA Inc. promptly took the precautionary step of issuing a voluntary recall of the affected product by removing the product in question from warehouses, working with retailers to ensure the product is removed from store shelves, and proactively notifying consumers.

Kao USA cares about our consumers’ safety. We are committed to manufacturing products that not only meet, but exceed, the highest industry standards.

The amount of recalled product is limited to two sizes offered for Jergens® Ultra Healing Moisturizer. Only specific lots of the 3 oz and 10 oz sizes are affected.

IDENTIFYING THE AFFECTED PRODUCTS

• Jergens® Ultra Healing Moisturizer, manufactured between October 1, 2021 and October 18, 2021, could be impacted.
• The affected lot codes for the 3 oz size (UPC 019100109971 for single bottles and 019100267114 for pack of 3) can be found on the back of the bottle printed in black ink and begin with the prefix “ZU”:

ZU712851	ZU712871
ZU712911	ZU722881
ZU712861	ZU712881
ZU722851

• The affected lot codes for the 10 oz size (UPC 019100109988) can be found on the bottom of the bottle printed in black ink and begin with the prefix “ZU”:

ZU722741	ZU722781
ZU732791	ZU732811
ZU722771	ZU732781
ZU732801	ZU732821

Kao USA Inc. will inform regulatory authorities of the issue and we are working with our partners on improved cleaning and sanitization practices so that similar issues can be prevented in the future.

Anyone who has product from a recalled lot should call the Kao USA Inc. Consumer Care Center for a free product coupon at the following number: 1.800.742.8798 or send an email to: consumer@kao.com. (Hours of operation: Monday – Friday, 9AM – 5PM US ET) A postage paid label and plastic bag will be sent to consumers via mail to easily return the product.

Any adverse events with the use of this product should be reported via the FDA’s MedWatch Program by one of the following methods:

By phone at 888.463.6332

** The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) chicken salad product containing a Food and Drug Administration (FDA) regulated salad dressing that has been recalled by the producer due to concerns that the salad dressing may contain hard plastic.  FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed.

The chicken salad product items were produced on 3/03/22, 3/04/22, 3/05/22, and 3/06/22. The following product is subject to the public health alert [view label here]:

• 12-oz. plastic tray packages containing “Trader Joe’s CRUNCHY SLAW with Chicken, Crispy Noodles & Peanut Dressing” and a use by date of 03/09/22, 03/10/22, 03/11/22, or 03/12/22 printed on the label.

The products bear establishment number “P-6247” inside the USDA mark of inspection. These items were shipped to retail locations in Arizona, California, Nevada, New Mexico, and Utah.

The problem was discovered when an FSIS inspected establishment received notification from their salad dressing supplier that the salad dressing, which is regulated by FDA, may contain hard plastic. The establishment then notified FSIS of the issue. FSIS and FDA are coordinating on this issue.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider. Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

** March 7, 2022 – Fresenius Kabi USA is voluntarily recalling seven lots of Sodium Acetate Injection, USP, 400 mEq/100 mL (4 mEq/mL), 100 mL fill in a 100 mL vial to the user level due to the presence of particulate matter found in reserve and/or stability sample vials. Microscopic and elemental analyses determined the presence of particulates composed of carbon and oxygen with varying amounts of iron and trace amounts of sodium, silicon, chromium, aluminum and cellulose.

The administration of an injectable product that contains particulate matter may result in local irritation or swelling or infection in response to the foreign material.  If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death.  To date, no adverse event reports have been received for these recalled lots, which were produced and sold in 2020 and 2021.

Sodium Acetate Injection, USP is indicated as a source of sodium, for addition to large volume IV fluids to prevent or correct low blood sodium levels in patients with restricted or no oral intake. It is also useful as an additive for preparing specific IV fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions. Listed below is a table of the recalled lots distributed nationwide to wholesalers, distributors, hospitals, and pharmacies between September 2020 and November 2021. An image of the product packaging is also included below. 

Product Name/Product size	NDC Number	Product Code	Batch Number	Expiration Date	First Ship Date	Last Ship Date
Sodium Acetate Injection, USP, 400 mEq/ 100 mL (4 mEq/mL), 100 mL fill in a 100 mL vial	63323-032-00	322100	6124193	05/2022	09/08/2020	12/22/2020
6124196	05/2022	11/16/2020	01/27/2021
6124226	05/2022	12/22/2020	03/22/2021
6124532	06/2022	01/27/2021	04/13/2021
6125333	12/2022	04/06/2021	06/01/2021
6125678	01/2023	06/23/2021	09/27/2021
6126846	08/2023	10/07/2021	11/17/2021

Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lots, and to return the product to Fresenius Kabi. The recall letter and response form are available at https://www.freseniusExternal Link Disclaimer–External Link Disclaimerkabi.com/us/pharmaceuticalExternal Link Disclaimer–External Link DisclaimerproductExternal Link Disclaimer–External Link DisclaimerupdatesExternal Link Disclaimer.External Link Disclaimer

Customers with questions regarding this recall may contact Fresenius Kabi at 1-866-716-2459 Monday through Friday, during the hours of 8:00 a.m. to 5:00 p.m. Central Time. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.

** B. Braun Medical Inc. (B. Braun) is voluntarily recalling five (5) lots of 0.9% Sodium Chloride for Injection USP 250ML in Excel within the United States to the hospital/user level. The voluntary recall has been initiated due to fluid leakage or low fill volume of the respective containers.

The biggest risk with a slow leak in any intravenous solution preparation is a break in sterility which poses a risk for the patient being exposed to a bacterial or fungal infection. There is a remote probability this could lead to bloodstream infection. B. Braun has not received any reports of adverse events related to this recall.

0.9% Sodium Chloride for Injection USP in Excel is indicated for extracellular fluid replacement, treatment of metabolic alkalosis in the presence of fluid loss and mild sodium depletion. 0.9% Sodium Chloride Injection USP in Excel is also indicated for use as a priming solution in hemodialysis procedures and may be used to initiate and terminate blood transfusions without hemolyzing red blood cells.

Product Catalog Number:	Lot Number:	NDC:	Product Description:	Distribution Date Range:	Expiration Date:	Region Distributed:
L8002
J1E086	0264-7800-20	0.9% NACL INJ USP 250ML	15JUN2021 – 22JUL2021	31-May-23	United States
J1E204	0264-7800-20	0.9% NACL INJ USP 250ML	17JUN2021 – 21JUL2021	31-May-23	United States
J1E213	0264-7800-20	0.9% NACL INJ USP 250ML	02JUN2021 – 28JUN2021	31-May-23	United States
J1H137	0264-7800-20	0.9% NACL INJ USP 250ML	14JUL2021 – 20OCT2021	30-Jun-23	United States
J1H138	0264-7800-20	0.9% NACL INJ USP 250ML	14JUL2021 – 29OCT2021	30-Jun-23	United States

Product was distributed Nationwide within the United States to domestic distributors.

B. Braun is notifying its distributors and customers by an official recall notice sent via certified registered mail and is arranging for return of all recalled products. Facilities and distributors that have product which is being recalled should discontinue use immediately and contact the B. Braun Medical Inc. Customer Support Department at 800-227-2862 Monday through Friday, 8 a.m. – 6 p.m. EST to arrange for product return.

Facilities with questions regarding this recall can contact B. Braun by phone at 800-227-2862 Monday through Friday, 8 a.m. – 6 p.m. EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

**

** Boyd Specialties, LLC, a Colton, Calif. establishment, is recalling approximately 1,634 pounds of ready-to-eat (RTE) jerky products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The multiple jerky products were produced on February 23, 2022. The products subject to the recall can be found here, and the labels can be found here.

The products subject to recall bear establishment number “EST. 40269” inside the USDA mark of inspection. These items were shipped to retail locations in Alabama, California, Connecticut, Michigan, New Jersey, North Carolina, Pennsylvania, and Texas.                          

The problem was discovered by FSIS during follow-up procedures after a routine FSIS product sample confirmed positive for Listeria monocytogenes.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  

Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ pantries. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media and consumers with questions regarding the recall can contact Anthony Middleton, Production Manager at Boyd Specialties, at (909) 219-5120.

 

March 1

1781 – Formal ratification of the Articles of Confederation was announced by Congress. Under the Articles, Congress was the sole governing body of the new American national government, consisting of the 13 original states. The Articles remained in effect through the Revolutionary War until 1789, when the current U.S. Constitution was adopted.

March 30

1855 – About 5,000 “Border Ruffians” from western Missouri invaded the territory of Kansas and forced the election of a pro-slavery legislature. It was the first election in Kansas.

1958 – The Alvin Ailey American Dance Theater gave its initial performance.

 1981 – Newly elected President Ronald Reagan was shot in the chest while walking toward his limousine in Washington, D.C., following a speech inside a hotel. The president was then rushed into surgery to remove a 22-caliber bullet from his left lung. “I should have ducked,” Reagan joked. Three others were also hit including Reagan’s Press Secretary, James Brady, who was shot in the forehead but survived. The president soon recovered from the surgery and returned to his duties.

1909 – In Oklahoma, Seminole Indians revolted against meager pay for government jobs.

1939 – The comic book “Detective Comics #27” appeared on newstands. This comic introduced Batman.

1981 – U.S. President Ronald Reagan was shot and wounded in Washington, DC, by John W. Hinckley Jr. Two police officers and Press Secretary James Brady were also wounded.

Birthday – Vincent Van Gogh (1853-1890) was born in Groot Zundert, Holland. He was a Postimpressionist painter, generally considered the greatest Dutch painter after Rembrandt. During his short (10-year) painting career he produced over 800 oil paintings and 700 drawings, but sold only one during his lifetime. In 1987, the sale of his painting Irises brought $53.9 million, the highest price ever paid for a work of art up to that time. During his life, Van Gogh suffered from despair and bouts of mental illness, at one point cutting off part of his own left ear. He committed suicide in 1890 by gunshot.

March 31

1945 – “The Glass Menagerie” by Tennessee Williams opened on Broadway.

1776 – Abigail Adams wrote to her husband John that women were “determined to foment a rebellion” if the new Declaration of Independence failed to guarantee their rights.

 1933 – The Civilian Conservation Corps, the CCC, was founded. Unemployed men and youths were organized into quasi-military formations and worked outdoors in national parks and forests.

 1968 – President Lyndon Johnson made a surprise announcement that he would not seek re-election as a result of the Vietnam conflict.

1885 – Binney & Smith Company was founded in New York City. The company later became Crayola, LLC.

1889 – In Paris, the Eiffel Tower officially opened.

1870 – In Perth Amboy, NJ, Thomas Munday Peterson became the first black to vote in the U.S.

1902 – In Tennessee, 22 coal miners were killed by an explosion.

1904 – In India, hundreds of Tibetans were slaughtered by the British.

1908 – 250,000 coal miners in Indianapolis, IN, went on strike to await a wage adjustment.

1900 – In France, the National Assembly passed a law reducing the workday for women and children to 11 hours.

 1991 – The Soviet Republic of Georgia, birthplace of Josef Stalin, voted to declare its independence from Soviet Russia, after similar votes by Lithuania, Estonia and Latvia. Following the vote in Georgia, Russian troops were dispatched from Moscow under a state of emergency.

Birthday – Boxing champion Jack Johnson (1878-1946) was born in Galveston, Texas. He was the first African American to win the heavyweight boxing title.

(Photo and picture credits: Library of Congress and U.S. National Archives)

The 1799 gradual abolition law declared that children born after July 4, 1799 to enslaved mothers in New York would be born free, but would have to provide free services to their mothers’ masters until they reached 25 if female and 28 if male.

history.nycourts.gov