** Daiso Issues Allergy Alert for Prepackaged Snacks
Daiso California LLC of La Mirada, CA is recalling the below listed snacks due of undeclared allergen ingredients. People who have an allergy or severe sensitivity to soybeans and milk run the risk of serious or life-threatening allergic reaction if they consume these products.
These prepackaged snacks were sold in Daiso stores in California, Washington, Nevada, Texas, New York, and New Jersey.
There have been no reported cases of allergic reaction to these products. The recall was initiated after it was discovered that packaging did not adequately disclose the presence of all allergens. Sale of the products have been suspended, and Daiso California has pulled the products from store shelves
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** 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 small local produce distributors or wholesalers for further distribution to retail stores within CA and HI.
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 #3779 outside of box.
No illnesses have been reported to date in connection with this problem. The distribution of the product is suspended.
The recall was the result of a routine sampling program by the State of Hawaii which revealed that the finished products contained Listeria monocytogenes. We have ceased the production and distribution of the product as we continue our investigation as to what caused the problem.
This recall is being made with the knowledge of the U.S. Food and Drug Administration and CDPH.
Although safety measures were taken to prevent the following risk, the safety of consumers is our top priority. We urge to return enoki package 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.
** February 23, 2023, Global Pharma Healthcare is voluntarily recalling Batch No. H29 of Artificial Eye Ointment, distributed by Delsam Pharma to the consumer level, due to possible microbial contamination. Additionally, some product packaging is leaking or may otherwise be compromised.
Risk Statement: Use of contaminated eye ointment may cause adverse events, including infection in the eye that could lead to blindness. To date, Global Pharma Healthcare has not received any reports of adverse events related to this product.
Artificial Eye Ointment (mineral oil 15%, white petrolatum 83%, 3.5 grams / 1/8 oz.) is used as an eye lubricant and to relieve dryness of the eyes. The affected product is packaged in a white aluminum tube within a paper carton. The product can be identified by the photos provided below. The product was distributed nationwide in the United States, and by Delsam through internet retail sites. Delsam Pharma’s NDC for this product is 72570-122-35, and its UPC code is 3 72570 012235 3.
Global Pharma Healthcare is notifying the brand owner and importer of this product, Delsam Pharma, about this recall, and is requesting that wholesalers, retailers, and customers who have the recalled product should stop any use and discard the product safely and appropriately.
Consumers with questions regarding this recall can contact the distributor Delsam Pharma, LLC by phone at 1-866-826-1306 or by e-mail at delsampharma@yahoo.com from Monday to Friday from 11am to 4pm EST.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these over-the-counter drug products.
** Kawasho Foods USA Inc. of New York, NY, is voluntarily recalling one lot of canned GEISHA Medium Shrimp 4oz. because of reported swelling, leaking, or bursting cans. There is a possibility that the product has been under processed, which could lead to the potential for spoilage organisms or pathogens.
The Product was distributed to retail stores (Walmart, Associated Food Stores, Stater Bros Markets, Safeway, Albertsons) in California, Utah, Arizona, and Colorado.
The GEISHA Medium Shrimp is packaged in a 4oz. metal can, with UPC 071140003909. The one lot being recalled is LGC12W12E22; BEST BY: MAY/12/2026 and this code appears on the bottom of the product can.
Consumers should not use this product, even if it does not look or smell spoiled. No illnesses or other adverse consequences have been reported to date in connection with this product.
Consumer who have purchased this product are urged to return to place of puchase for a full refund. If you have any question regarding this recall, please contact us at (212)841-7400 (Monday to Friday, 9:00 a.m. to 5 p.m. EST) or via email at info@geishabrand.com.
** Bindle Bottle LLC of Carlsbad, CA, is recalling its Bindle Bottles because they may contain an area of exposed lead located in the bottom storage compartment of the bottle. Unpackaged food stored in the bottom storage compartment of the bottle may have been adulterated by the lead and could pose health problems to people or animals eating that adulterated food. People with high blood levels of lead may show no symptoms, but the condition may cause damage to the nervous system and internal organs. Acute lead poisoning may cause a wide range of symptoms, including abdominal pain, muscle weakness, nausea, vomiting, diarrhea, weight loss, and bloody or decreased urinary output. Children are particularly vulnerable to lead poisoning. If a child is exposed to enough lead for a protracted period of time (e.g., weeks to months) permanent damage to the central nervous system can occur. This can result in learning disorders, developmental defects, and other long-term health problems. Clinical signs in dogs with acute lead poisoning may include lethargy, anorexia, behavioral changes, ataxia (wobbly gait), tremors, and seizures.
The recalled Bindle Bottles were distributed nationwide via bindlebottle.com, amazon.com, promotional distributors, and in retail stores.
The product comes in four sizes: 32 oz, 24 oz, 20 oz, and 13 oz. Bindle Bottle is also recalling the 24 oz bottle that is part of the Puppy Pack.
No illnesses have been reported to date in connection with this problem.
Reports by Lead Free Mama and Consumer Reports led the firm to have the bottle tested. The recall was initiated after analytical results revealed that the small, 0.4” diameter soldering dot in the bottom storage compartment contained lead. Subsequent investigation indicates the problem was caused by a lack of a cover or barrier to the exposed soldering dot.
Production of Bindle Bottles has been suspended and will be overhauled going forward, eliminating the presence of exposed lead anywhere on future products.
As part of the recall, consumers who purchased a Bindle Bottle are eligible to receive at-home repair kits to rectify the issue. These repair kits can be obtained by filling out a form at bindlebottle.com/pages/recallExternal Link Disclaimer. Consumers with questions may contact the company at product_safety@bindlebottle.com
** Delight Foods USA LLC Recalls Ineligible Frozen Siluriformes Products Imported from India
Delight Foods USA LLC, a distributor and the Importer of Record located in Jersey City, N.J., and Delight Foods LLC, a distributor and the Importer of Record located in San Jose, Calif., is recalling approximately 2,961 pounds of imported frozen Siluriformes (catfish) products. The products were imported from India, a country ineligible to export Siluriformes products to the United States.
In the news release dated July 29, 2022, and titled, Edgewell Personal Care Issues Voluntary Nationwide Recall of Banana Boat Hair & Scalp Sunscreen Due to the Presence of Benzene, one additional lot code (“20301CF”) has been added to the recall. The modified announcement follows:
SHELTON, Conn., January 27, 2023 Edgewell Personal Care Company (NYSE: EPC) today expanded its voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the table below. One additional batch has been added to the original recall announced on July 29, 2022. A review found that some samples of the product contained trace levels of benzene. While benzene is not an ingredient in any Banana Boat products, the review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can.
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** The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen chicken products due to misbranding and an undeclared allergen. The product contains cashews, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to cashews are aware that these products should not be consumed. A recall was not requested because it is believed that the products are no longer available for consumers to purchase.
The frozen products are labeled as Chicken Korma with Basmati Turmeric Rice but may contain Vegetable Tikka Masala with Turmeric Rice. This item was produced on November 8, 2022. The following product is subject to the public health alert [view labels]:
- 10-oz. containers of “Wegmans Chicken Korma with Basmati Turmeric Rice” with Best By 08 NOV 2023.
The products subject to the public health alert bear establishment number “P-34641” inside the USDA mark of inspection. These items were shipped to retail locations in New York and Pennsylvania.
The problem was discovered when the producing establishment notified FSIS that they received consumer complaints reporting that product labeled as chicken korma actually contained vegetable tikka masala. The vegetable tikka masala contains cashews not declared on the chicken korma product label.
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 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.
Consumers and members of the media with questions about the public health alert can contact Giovanni Gomez, Director of Business Development, Cafe Spice, at 845-863-0910 or Giovanni@cafespice.com.
The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that not-ready-to-eat meat products were subject to temperature abuse during storage at a distribution center prior to delivery to retailers, which may have resulted in the growth of spoilage organisms or pathogens. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
** Fresh Ideation Food Group LLC Recalls Sandwiches and Other Products Because of Possible Health Risk
Fresh Ideation Food Group LLC of Baltimore, MD is recalling products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated withListeria monocytogenesan 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,Listeriainfection can cause miscarriages and stillbirths among pregnant women.
Products have been distributed in Connecticut, District of Columbia, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia. Recalled Products were sold in retail locations, vending machines, and during travel with transportation providers. The products include sandwiches, salads, snacks, yogurt, wraps and related products. A listing of the relevant product information is provided at the bottom of this press release.
** Conagra Brands, Inc., a Fort Madison, Iowa establishment, is recalling approximately 2,581,816 pounds of canned meat and poultry products due to a packaging defect that may cause the products to become contaminated without showing any outward signs of contamination, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The meat and poultry products were produced between December 12, 2022, and January 13, 2023. The following products are subject to recall: [view spreadsheet] [view labels].
The products subject to recall bear establishment number “P4247” on the product cans. These items were shipped to retail locations nationwide.
The problem was discovered when the establishment notified FSIS after observing spoiled and/or leaking cans from multiple production dates at the establishment’s warehouse.
Subsequent investigation by the establishment determined that the cans subject to recall may have been damaged in a manner that is not readily apparent to consumers, which may allow foodborne pathogens to enter the cans.
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 on retail shelves or in consumers’ pantries. 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 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 lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Members of the media with questions about the recall can contact Dan Hare, Senior Director of Communications, ConAgra Brands, at 312-549-5355 or daniel.hare@conagra.com. Consumers with questions about the recall can call 800-289-6014, Monday-Friday 9 a.m. to 5 p.m. CST or email consumer.care@conagra.com.
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