Food & Beverage Recalls
Healthwest Minerals Inc. DBA Mt Capra Products Recalls Goat Milk Formula Recipe Kit and Warns Consumers Against the Use of Product as Infant Formula
May 10, 2024 – Healthwest Minerals, Inc. d/b/a Mt. Capra Products of Chehalis, Washington, is recalling 1,506 boxes of Goat Milk Formula Recipe Kit on the recommendation of the Food and Drug Administration (FDA) and advises consumers to immediately discontinue use of the product as infant formula. The FDA is concerned that the formula does not meet all FDA requirements for infant formula, does not provide sufficient nutrition when used as an infant formula, and the storage instructions may be insufficient for the product. Infants consuming the recalled product without additional iron supplementation can develop iron deficiency anemia and feeding intolerance.
The Goat Milk Formula Recipe Kit 10 lb 8 oz was sold through Mt. Capra’s web store (mtcapra.com) or one retail store in Chehalis, Washington, from 05/01/23 to 05/01/24.
Western Mixers Produce & Nuts, Inc. Recalls Yogurt Covered Pretzels Because of Possible Health Risk
Western Mixers Produce & Nuts, Inc. of Ontario, CA is recalling Yogurt Covered Pretzels, because the yogurt coating 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.
Yogurt Covered Pretzels was distributed in the State of California, through Thorp Fruit, Down Home Goods, Smart & Final, Gelson’s retail stores.
DaVinci Laboratories Issues Allergy Alert on Undeclared Shellfish Allergen in Amyloid Complete Product Lot 549853001
DaVinci Laboratories, a division of FoodScience, LLC of Williston, Vermont is recalling 72 bottles of Amyloid Complete because it may contain undeclared shellfish (Shrimp and Crab). People who have an allergy or severe sensitivity to shellfish run the risk of serious or life-threatening allergic reaction if they consume these products.
Amyloid Complete product was distributed nationwide through e-commerce (iHerb.com, fullscripts.com) and direct delivery.
Product is contained in a white plastic bottle marked with lot # 549853001 and 0125 expiration date on the side of the label. Amyloid Complete is a capsule that is tan in color.
Texas Pecan Issues Allergy Alert on Undeclared Tree Nuts (Not Named Individually), Soy, Dairy(Milk), Sesame and Wheat Not Named in Product
Texas Pecan of Dallas TX is recalling 1 Lb and 8 oz products because it may contain an undeclared allergen. People who have an allergy or severe sensitivity to( tree nuts, peanuts, almonds, brazils, cashews, filberts, macadamias, pistachios, pecans, pine nuts, walnuts, soy, dairy (milk), sesame and wheat), run the risk of serious or life threating allergic reaction if they consume these products. This company has been in business for over 40 years and no sickness or allergic reaction has ever been reported to us.
This product could have been bought at our retail location or thru our web site(www.texaspecanco.com). It it only the 1 lb and 8 oz bags with lot numbers found on the bottom left corner ranging from 23200-23265 and 24001-24079. All bags are a clear poly bag with our Texas Pecan label on them. There have not been any reports of related illness or allergic reactions to any of the product ever purchased at Texas Pecan.
Palmer Candy Company Recalls White Confectionary Products Because of Possible Health Risk
Palmer Candy Company, Sioux City, Iowa, is recalling its “White Coated Confectionary Items” because they 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 recalled Confectionary Items were distributed nationwide in retail stores and to wholesale.
The recalled confectionary items were distributed nationwide in Walmart, HyVee, Target, Dollar General, and to distributors in Alabama, California, Florida, Illinois, Iowa, Kansas, Missouri, Nebraska, North Dakota, Oregon, Pennsylvania, South Carolina, South Dakota, Texas, Virginia, Wisconsin and Wyoming.
Recall_Supplier Recalls Impact Two Hy-Vee Products Third-Party Manufacturers Alert Retailer of Potential for Contamination; No Illnesses Reported
WEST DES MOINES, Iowa (May 6, 2024) — Hy-Vee, Inc., based in West Des Moines, Iowa, is voluntarily recalling two varieties of its Hy-Vee Cream Cheese Spread out of an abundance of caution due to the potential for contamination with Salmonella. Additionally, Hy-Vee is voluntarily recalling its bulk-packaged Cookies & Cream Mix out of an abundance of caution due to the potential for contamination with Salmonella.
These products are manufactured at different third-party facilities around the Midwest and are sold under HyVee’s private label and bulk packaging programs. The manufacturers of these products notified Hy-Vee of the potential issue and out of an abundance of caution Hy-Vee is voluntarily recalling these specific products. There have been no confirmed reports of adverse reactions due to consumption of any of these products.
The affected products were distributed to Hy-Vee, Hy-Vee Drugstore and Dollar Fresh Market locations – as well as Hy-Vee Fast and Fresh convenience stores – across the company’s eight-state region of Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.
Medical Device Recalls
MEGADYNE™ Initiates Global Discontinuation and Voluntary Recall of MEGA SOFT™ Pediatric Patient Return Electrode
Cincinnati, OH – May 10, 2024 – MEGADYNE™ is initiating a voluntary recall of all MEGADYNE™ MEGA SOFT™ Pediatric Patient Return Electrodes. The product is being removed because Megadyne has received reports of patient burn injuries in procedures where the Mega Soft Patient Return Electrodes were used. A root cause investigation on the reports included testing which showed a combination of factors when present together may result in potential for thermal injuries.
The combination of these conditions may be more likely when the pad is used with infants and small children. Because the pediatric pad is designed for patients between 0.8 to 50 pounds, which would be predominantly patients under the age of 12, the decision was made to discontinue and recall the 0840 pediatric pad product.
Between 2018 and today, there have been 4 reported injuries and no reports of death associated with this product. The Company has decided to discontinue and voluntarily recall the MEGADYNE™ MEGA SOFT™ Pediatric Patient Return Electrode. U.S. (Food and Drug Administration) FDA has been notified of this action.
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