• Recall Notification Report 058-2018 (Pork Products)

  Nueske’s Meat Products, Inc., a Wittenberg, Wis. establishment, is recalling approximately 12,946 pounds of pork products due to misbranding.

• Updated information is now available. The lists of retail consignees have been posted for recalls:
  • 055-2018, People’s Sausage Co. Recalls Jerky and Meat Stick Products Produced without an Approved Voluntary Grant of Inspection (June 25, 2018)
• L&D Market, Inc. Recalls Chicken Wrap Products Due to Misbranding and Undeclared AllergensL&D Market, Inc., a Boston, Mass. establishment, is recalling approximately three pounds of chicken wrap products due to misbranding and undeclared allergens.
• People’s Sausage Co. Recalls Jerky and Meat Stick Products Produced without an Approved Voluntary Grant of InspectionPeople’s Sausage Co., a Los Angeles, Calif. establishment, is recalling approximately 13,554 pounds of elk, bison and beef meat stick products that were produced without an approved voluntary grant of inspection.
• Talking Rain® (the Company) is voluntarily recalling specific lot codes of bottles of its Sparkling Ice® Cherry Limeade beverage in response to a small number of customer complaints that reported an off-taste and off-odor of the affected product. The Company made the decision to recall the product out of an abundance of caution. No other Sparkling Ice products are affected by this recall.The Sparkling Ice Cherry Limeade product subject to recall was produced only at one of the Company’s facilities that make this product. The product comes in a 17 ounce clear plastic bottle under the name Sparkling Ice Cherry Limeade. The product is sold as a single item, as well as in multipacks of the affected product and in multipacks containing a variety of other unaffected flavors. The product subject to recall can be identified by the following information that is displayed on the neck of the bottle. All other products made by the Company are not part of this voluntary recall.Affected product labeling:

  Bottle Lot Code	Expiration Date on Bottle	Expiration Date	Bottle UPC	Case/Variety Pack UPCs
  8064-63	120518	12/5/18	01657195084	016571950866
  8065-63	120618	12/6/18		016571950927
  8079-63	122018	12/20/18		016571951283
  8080-63	122118	12/21/18		016571950866
  8087-63	122818	12/28/18		016571953126
  8088-63	122918	12/29/18		016571953614
  8089-63	123018	12/30/18
  8112-63	012219	01/22/19
  8113-63	012319	01/23/19
  8114-63	012419	01/24/19
  8118-63	012819	01/28/19
  8119-63	012919	01/29/19
  8126-63	020619	02/06/19
  8131-63	021119	02/11/19
  8132-63	021219	02/12/19
  8144-63	022419	02/24/19
  8145-63	022519	02/25/19
  8146-63	022619	02/26/19
  8165-63	031419	03/14/19
  8166-63	031519	03/15/19
  8167-63	031619	03/16/19

  Talking Rain learned of the issue after a small number of customers brought their concerns to the company’s attention. Talking Rain is currently investigating the cause of the issue in collaboration with the U.S. Food and Drug Administration (FDA).

  Consumers who purchased the affected product are advised not to drink it and to call the Talking Rain customer center at 855-201-4333 to receive a coupon to replace their purchase.

• Aunt Kitty’s Foods Inc. Recalls Canned Chicken Products Due to Possible Processing DeviationAunt Kitty’s Foods, Inc., a Vineland, N.J. establishment, is recalling approximately 10,805 pounds of canned chicken gravy products due to a possible processing deviation that may have led to underprocessing of products.
• Updated information is now available. The lists of retail consignees have been posted for recalls:
  • 051-2018, Texas Natural Meats Recalls Frozen Raw Ground Beef Products (June 20, 2018)
•  Updated information is now available. The lists of retail consignees have been posted for recalls:
  • 053-2018, Quay Corporation Recalls Pork Products Produced Without Benefit Of Inspection (June 22, 2018)
• Quay Corporation Recalls Pork Products Produced Without Benefit Of InspectionThe Quay Corporation, a Skokie, Ill. establishment, is recalling approximately 258,121 pounds of pork lard products that were produced without the benefit of federal inspection.
• Kellogg Company today announced it is voluntarily recalling 15.3 oz. and 23 oz. packages of Kellogg’s ® Honey Smacks ® cereal (with code dates listed below) because these products have the potential presence of Salmonella. No other Kellogg products are impacted by this recall.Kellogg launched an investigation with the third-party manufacturer who produces Honey Smacks immediately after being contacted by the Food & Drug Administration (FDA) and Centers for Disease Control (CDC) regarding reported illnesses.According to the CDC, use or consumption of products contaminated with Salmonella may result in serious illness. It can also produce serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy individuals infected with Salmonella can experience fever, diarrhea, nausea, vomiting and abdominal pain. The illness usually lasts four to seven days, and most persons recover without treatment. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses.HOW TO IDENTIFY THE RECALLED PRODUCTThe affected product includes the following varieties distributed across the United States as well as limited distribution in Costa Rica, Guatemala, Mexico, the Caribbean, Guam, Tahiti and Saipan. The BEST if Used By Date can be found on the top of the cereal box, and the UPC code can be found on the bottom of the box.

  Description (Retail)	UPC Code	Size	BEST If Used By Date
  Honey Smacks (with limited distribution outside the U.S.)	3800039103	15.3 oz	JUN 14, 2018 through JUN 14, 2019
  Honey Smacks	3800014810	23 oz	JUN 14, 2018 through JUN 14, 2019

  Kellogg is asking that people who purchased potentially affected product discard it and contact the company for a full refund. Consumers seeking more information, including images of these products, can visit kelloggs.com/honeysmacksrecall or call 1-800-962-1413 from Monday – Friday, from 9 a.m. to 6 p.m. ET as well as Saturday and Sunday from 10 a.m. – 4 p.m. ET.

  Link to Outbreak Summary

• Various Aortic Endovascular Graft Systems: Letter to Health Care Providers – UPDATE on Type III Endoleaks intended for: Risk Manager, Surgery, Patient, Cardiology was just added to the FDA MedWatch Webpage.
  You can read the complete MedWatch Safety Alert that includes recommendations at:https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm611193.htm
• Gaia Ethnobotanical, LLC., is voluntarily recalling all kratom (mitragyna speciosa) powder products, with Lot No.: 0102031800 it manufactured, processed, packed, and/or held, between March 18, 2018 to March 30, 2018 to the consumer level. The products have been found by the U.S. Food and Drug Administration (“FDA”) via sample testing and finding to have salmonella contamination. In lieu of such FDA findings the company has implemented standard operating procedures and sterilization processes in accordance to FDA guidelines.These products have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.The affected products (listed below) can be identified by Lot No.: 0102031800 and Batch No.: 031800. Specifically, the products were distributed to AK, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM NV, NY, OH, OK, OR, PA, PR, SC, SD, TX, VA, WA, WY via the internet.

  Label	Size	Packaging
  Gaia Ethnobotanical Bali Gold	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Elephant	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Ganesh MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green Dragon	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green Horn	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green Kapuas Hulu	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green Malay	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Green Thai	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Plantation Green MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Plantation Red MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Plantation White MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Purple 8-1	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Bali	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Borneo	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Dragon	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Horn	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Kapuas Hulu	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Red Thai	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Super Green Malay	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical White Borneo	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical White Horn	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical White MD	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical White Thai	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Yellow Thai	1oz, 250g, 1kg	Plastic Bag
  Gaia Ethnobotanical Yellow Vietnam	1oz, 250g, 1kg	Plastic Bag

  Gaia is notifying its customers by e-mail and/or telephone and are urged to return the recalled products to us or immediately discard them.

  Consumers with questions regarding this recall can contact the company at  fdarecall@gaiaethnobotanical.com or call 24/7 at 702-996-8523.

• Agri Star Meat And Poultry LLC Recalls Beef Pastrami Products due to Possible Processing DeviationAgri Star Meat and Poultry LLC, a Postville, Iowa establishment, is recalling approximately 3,592 pounds of ready-to-eat (RTE) beef pastrami products due to processing deviations that may have led to underprocessing of products and resulted in inadequate curing.
• NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is recalling its NOW Real Food® Zesty Sprouting Mix – Product Code 7271, Lot #3031259 and Lot #3038165 – because its primary ingredient, Crimson Clover Seeds, has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.  Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.

Approximately 10,000 units of Zesty Sprouting Mix were distributed online and in retail stores nationwide since December 2017.

Recalled products include:

No other products are affected or are involved in this recall. No illnesses have been reported to date.

Evidence of potential contamination was implicated in ongoing FDA and CDC investigations into multistate outbreaks of Salmonella infections, of which the clover seed supplier was notified.

NOW has provided information on this recall to all its retailers who purchased this product and has encouraged retailers to make every effort to contact their customers to facilitate the return of affected products.

Consumers who have purchased the recalled Zesty Sprouting Mix should stop using the product immediately and return it to place of purchase for a full refund. Receipt is not required for refund.

Consumers with questions regarding this recall can contact NOW’s Customer Service Department by phone at 888-NOW-FOODS (888-669-3663) Monday through Friday, 8:00 a.m. to 6:00 p.m. Central time.

• Texas Natural Meats Recalls Frozen Raw Ground Beef ProductsTexas Natural Meats, a Lott, Texas establishment, is recalling approximately 489 pounds of frozen raw, ground beef products that may be contaminated with Shiga toxin-producing E. coli (STEC) O103.
• Golden Star Wholesale of Troy, MI 48084 is recalling, AL Reef  Dried Apricots Sour, because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.The recalled AL Reef  Dried Apricots Sour, 12 oz clear plastic container, un-coded were sold via retail stores in MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO between November 2017 and May 2018.No illnesses have been reported to date in connection with this problem.The recall was initiated after routine sampling of the product by New York State Department of Agriculture and Markets food inspectors and subsequent analysis by Department food laboratory personnel revealed the presence of undeclared sulfites in Al Reef Dried Apricot Sour package that did not declare sulfites on the label.Consumers who have purchased AL Reef Dried Apricot Sour should return it to the place of purchase. Consumers with questions may contact the company at 248-577-5080.
• CORAL GABLES, FL. – Del Monte Fresh Produce N.A., Inc. (“Del Monte Fresh”) announced today, the voluntary recall of a limited quantity of 6 oz., 12 oz. and 28 oz. vegetable trays containing fresh broccoli, cauliflower, celery sticks, carrots, and dill dip sold to select retailers in Illinois, Indiana, Iowa, Michigan, Minnesota and Wisconsin. Del Monte was notified by state agencies of the outbreak and its potential involvement. Del Monte has recalled the products because they may be linked to this recent cluster of illnesses and have the potential to be contaminated with Cyclospora, a parasite that can cause the intestinal illness Cyclosporiasis. According to the Centers for Disease Control, the infection usually is not life threatening. Symptoms of Cyclosporiasis may include the following: watery diarrhea (most common), loss of appetite, weight loss, cramping, bloating, increased gas, nausea, fatigue. Other symptoms that may occur but are less common include the following: vomiting and/or low-grade fever.The recalled products were distributed to: Kwik Trip, Kwik Star, Demond’s, Sentry, Potash, Meehan’s, Country Market, Food Max Supermarket and Peapod in Illinois, Indiana, Iowa, Michigan, Minnesota, and Wisconsin and have “Best If Enjoyed By” date of June 17, 2018 or earlier. The recalled products were distributed for sale in clear plastic containers with the following labels and markings:

  Product Name	Most Recent Best By date	Components	UPC Code
  Del Monte 6 oz. Veg Tray w/dip	6/17/2018	Baby carrots, broccoli, cauliflower and dill dip	7 1752472715 2
  Del Monte 12 oz. Veg Tray w/dip	6/17/2018	Baby carrots, broccoli, cauliflower and dill dip	7 1752472518 9
  Del Monte 28 oz. Small Veg Tray w/dip	6/17/2018	Baby carrots, broccoli, cauliflower, celery sticks and dill dip	7 1752478604 3

  Consumers who believe that they are in possession of any of the above products affected by this recall should dispose of the product in an appropriate waste container. For any inquiries, consumers may call 24 hour customer service line at 1-800-659-6500 or email Del Monte Fresh at Contact-US-Executive-Office@freshdelmonte.com.

  Outbreak Summary

• Winter Sausage Manufacturing Co. Recalls Poultry and Meat Products due to MisbrandingWinter Sausage Manufacturing Co, an Eastpointe, Mich. establishment, is recalling approximately 28,346 pounds of poultry, pork, and beef products due to misbranding.

• WASHINGTON, June 12, 2018 – J Bar B Foods, a Waelder, Texas establishment, is recalling approximately 410,985 pounds of beef brisket smoked sausage products due to an adulterated and misbranded ingredient, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain a pork casing, which is not declared on the product label, and may cause an allergic reaction in some individuals.

  The ready-to-eat beef brisket smoked sausage products were produced on various dates from June 21, 2016 to May 29, 2018. The following products are subject to recall: [View Label (PDF only)]

  • 12 oz. vacuum-packed packages of “H-E-B TEXAS HERITAGE SAUSAGE SMOKED WITH NATURAL HARDWOOD BEEF BRISKET.”

  Lot codes, packaging dates and other identifying label information may be found here.

  The products subject to recall bear establishment number “EST. 7066” inside the USDA mark of inspection. These items were shipped to retail locations in Texas.

  The problem was discovered on June 12, 2018 in response to a customer inquiry that a beef smoked sausage product did not specify pork casing as part of the ingredients statement.

  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.

  FSIS is concerned that some product may be frozen and in consumers’ freezers. 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.

  FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers.

  Consumers and members of the media with questions about the recall can contact Adam Bosi, president of J Bar B Foods at (860) 787-7511.

• Venda Ravioli, Inc. Recalls Meat and Poultry Pasta Products Produced without Benefit of InspectionVenda Ravioli, Inc., a Providence, R.I. establishment, is recalling approximately 738 pounds of frozen meat ravioli products that were produced without the benefit of federal inspection while the establishment was under suspension.
• 046-2018, Venda Ravioli, Inc. Recalls Meat Ravioli Products Produced Without Benefit of Inspection (June 8, 2018)
• Important advice for consumers and retailers in Georgia, Illinois, Indiana, Kentucky, Michigan, Missouri, North Carolina, and Ohio:
  • On June 8, 2018, Caito Foods, LLC recalled fresh cut watermelon, honeydew melon, cantaloupe, and fresh-cut fruit medley products containing one of these melons produced at the Caito Foods facility in Indianapolis, Indiana.
    • Recalled products were distributed to Georgia, Illinois, Indiana, Kentucky, Michigan, Missouri, North Carolina, and Ohio.
    • Recalled products were sold in clear, plastic clamshell containers at Costco, Jay C, Kroger, Payless, Owen’s, Sprouts, Trader Joe’s, Walgreens, Walmart, and Whole Foods/Amazon.
    • The investigation is ongoing to determine if products went to additional stores or states.
• Venda Ravioli, Inc. Recalls Meat Ravioli Products Produced Without Benefit of InspectionVenda Ravioli, Inc., a Providence, R.I. establishment, is recalling approximately 672 pounds of frozen meat ravioli products that were produced without the benefit of federal inspection.
• Tyson Foods Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter ContaminationTyson Foods Inc., a North Little Rock, Ark. establishment, is recalling approximately 3,120 pounds of frozen breaded chicken products that may be contaminated with extraneous materials, specifically blue and clear soft plastic
• Supermercado Selectos Recalls Raw, Frozen Siluriformes Fish, Meat and Poultry Products Produced Without Benefit of InspectionSupermercado Selectos, a San Sebastián, Puerto Rico firm, is recalling an undetermined amount of various raw, frozen Siluriformes fish, beef, pork and poultry products that were produced without the benefit of federal inspection.
• Goodman Food Products Recalls Fully Cooked Ground Beef Products Due to Possible Foreign Matter ContaminationGoodman Food Products, Texas, Inc., a Mansfield, Texas establishment, is recalling approximately 34,400 pounds of fully cooked ground beef products that may be contaminated with extraneous materials.
•  Liquid-filled Intragastric Balloons by Apollo Endosurgery and ReShape Lifesciences: Letter to Health Care Providers – New Labeling About Potential Risksintended for: Gastroenterology, Risk Manager, Health Professional, Patient was just added to the FDA MedWatch Webpage.
  You can read the complete MedWatch Safety Alert that includes recommendations at:   https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm609761.htm
• Hospira, Inc., a Pfizer company, is voluntarily recalling lots 72680LL and 76510LL of Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL, Carpuject Single-use cartridge syringe system (NDC 0409-1782-69), to the hospital/institution level due to the potential presence of embedded and loose particulate matter on the syringe plunger.In the event that impacted product is administered to a patient, the patient has a low likelihood of experiencing adverse events ranging from local irritation, allergic reactions, phlebitis, end-organ granuloma, tissue ischemia, pulmonary emboli, pulmonary dysfunction, pulmonary infarction, and toxicity. The risk is reduced by the possibility of detection, as the labeling contains a clear statement directing visual inspection of the product for particulate matter and discoloration prior to administration. To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots.Naloxone Hydrochloride, an opioid antagonist, is indicated for the complete or partial reversal of opioid depression. It is also indicated for the diagnosis of known or suspected opioid overdosage, and as an adjunctive agent for the management of septic shock. It is available as a sterile solution for intravenous (IV), intramuscular (IM), and subcutaneous (SC) administration. Naloxone is supplied in a Carpuject single-use cartridge with a 1 mL fill for use with the Carpuject syringe system.
  The NDC, Lot Number, Expiration Date, Strength and Configuration details for Naloxone Hydrochloride Carpuject Injection is indicated below. Product lots were distributed nationwide to wholesalers/distributors/hospitals in the United States, Puerto Rico, and Guam from February 2017 to February 2018.

  NDC	Number	Date	Strength	Configuration/Count
  0409-1782-03 (Single Unit) 0409-1782-69 (Box/Carton)	72680LL	1DEC2018	0.4 mg/mL 1 mL in 2.5mL	10-1 mL Single Use Carpuject&trad; (Sterile Cartridge Unit with Luer Lock) per box/carton; 100 boxes/cartons per case (1000)
  	76510LL	1APR2019	0.4 mg/mL, 1 ml in 2.5 mL

  Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers/ distributors/hospitals to arrange for return of any recalled product.
  Distributors or retailers with an existing inventory of the lots, which are being recalled, should stop use and distribution and quarantine immediately. Inform Healthcare Professionals in your organization of this recall. If you have further distributed the recalled product, to the wholesale or retail level, please notify any accounts or additional locations which may have received the recalled product from you. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.
  Healthcare Professionals with questions regarding this recall can contact Pfizer using the below information.

  Contact	Contact Information	Areas of Support
  Pfizer Medical Information	1-800-438-1985, option 3 (8am to 7pm ET Monday through Friday)	Medical Inquiries
  Pfizer Safety	1-800-438-1985, option 1 (24 Hours a day 7 days per week)	To report adver Events or product complaints

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

  Adverse events 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: www.fda.gov/medwatch/report.htm
  • Regular Mail or Fax: download form www.fda.gov/MedWatch/getforms.htm or call 1-800-FDA-1088 to request form, then complete and return address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• Supermercado Selectos Recalls Raw, Frozen Meat and Poultry Products Produced Without Benefit of Inspection Supermercado Selectos, a San Sebastián, Puerto Rico firm, is recalling an undetermined amount of various raw, frozen beef, pork and poultry products that were produced without the benefit of federal inspection.
• Committed to the quality of its products, H-E-B is voluntarily issuing an all-store recall for certain flavors and container sizes of EconoMax and Hill Country Fare ice creams and Creamy Creations sherbets for broken metal in processing equipment found during routine maintenance. The affected products were distributed to stores in Texas and Mexico.To date, there have been no injuries reported due to this incident.All products related to this recall have been removed from store shelves. H-E-B is working to have the products back on shelves as soon as possible.The voluntary recall impacts the following products:

  UPC Number	Product	Size	Best by date
  4122092736	EconoMax Neopolitan	4 quarts	6/1/2019 through 6/23/2019
  4122092733	EconoMax Neopolitan	56 ounces	6/24/2019
  4122092734	EconoMax Vanilla	4 quarts	5/24/2019 through 6/17/19
  4122092731	EconoMax Vanilla	56 ounces	5/26/2019 through 5/27/019
  4122090944	Hill Country Fare Chocolate	4.5 quarts	6/24/2019
  4122092215	Hill Country Fare Cookies and Cream	56 ounces	5/27/2019 through 5/28/2019
  4122090946	Hill Country Fare Fudge Revel	4.5 quarts	6/7/2019 through 6/8/2019
  4122090943	Hill Country Fare Neopolitan	4.5 quarts	6/3/2019 through 6/22/2019
  4122092212	Hill Country Fare Neopolitan	56 ounces	6/25/2019
  4122010102	Hill Country Fare Neopolitan (Mexico)	4.5 quarts	6/17/2019 through 6/18/2019
  4122090947	Hill Country Fare Strawberry Revel	4.5 quarts	6/8/2019 through 6/9/2019
  4122090942	Hill Country Fare Vanilla	4.5 quarts	6/6/2019 through 6/7/2019
  4122083898	HEB CC Fruit Punch Sherbet	Quart	12/22/2018
  4122034607	HEB CC Lime Sherbet	Quart	11/19/2018 through 11/20/2018

  Customers who purchased the product can return it to the store for a full refund. Customers with any questions or concerns may contact H-E-B Customer Service at 1-855-432-4438 Monday through Friday from 8 a.m. to 8 p.m. Central Standard Time.

• Ruiz Food Products, Inc. Recalls 12-Count Frozen Breakfast Burritos due to Possible Foreign Matter ContaminationRuiz Food Products, Inc., a Denison, Texas establishment, is recalling approximately 50,706 pounds of frozen breakfast burritos that may be contaminated with extraneous material.
• HeartWare HVAD System by Medtronic: Class I Recall – Due to Unintended Intermittent Electrical Disconnection between the Power Source and the Controller intended for: Cardiology, Risk Manager, Nursing, Patient was just added to the FDA MedWatch Webpage.

  You can read the complete MedWatch Safety Alert that includes recommendations at:https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm609599.htm