FDA Warning & Recall Information

Garden Grove, California-based LQNN, Inc., has recalled its Banh Ba Xa and several varieties of its Banh Pia, under multiple lot numbers and best-by dates, due to the potential presence of egg, an ingredient not declared on the product label. Individuals who live with an […]

Muskegon, Michigan-based Wesco, Inc. has recalled 750 units of its Wesco Mint No Bake Cookie Bites because it may contain traces of peanut, a major allergen not listed in the product’s ingredient list, according to the FDA. Individuals who live with a peanut allergy or […]

Following reports of adverse events linked to electrical operating room tables, the U.S. Food and Drug Administration (FDA) is emphasizing user training and advising healthcare providers to carefully follow instructions in the manufacturer’s product manual to mitigate risks to patients. Indicated to properly position a […]

On February 21, 2024, Avanos Medical, Inc., of Alpharetta, Georgia, announced a voluntary recall of certain lots of its MIC Gastric – Jejunal Feeding Tube Kits following Nurse Assist, LLC’s own voluntary recall of pre-filled syringes, among other sterile water products. Officials note that the […]

According to the FDA, Skokie, Illinois-based Raja Foods LLC has recalled its 3.5-ounce packages of “SWAD Cinnamon Powder” after learning that the product could contain traces of lead. While short-term and low-level exposure to lead is not believed to cause symptoms, those exposed may experience […]

Los Angeles, California-based Aji Mori Sauce Corp., doing business as Sushi Koo, has voluntarily recalled its Chillimami Sauce because it was not produced and distributed under the oversight of the California Department of Public Health (CDPH) Cannery Program. As such, FDA officials say that the […]

Consumers should be advised that Stokesdale, North Carolina-based KALO Foods, LLC has recalled its Single Slice Carrot Cake (under Universal Product Code 8 53407 00418 4) because the product has been found to contain soy, an allergen not listed in the label’s ingredient panel. Officials […]

The FDA is warning consumers that a corrective recall of Wipro GE Healthcare Private Ltd. Care Plus and Lullaby Incubators has been identified as Class I, the most serious type, because use of the devices has been found to pose a risk of serious injuries […]

According to the FDA, Los Angeles, California-based Backstage Center has recalled about 280 bottles of Alipotec Raiz de Tejocote dietary supplements bearing the “Alipotec King” sticker after an FDA analysis revealed the product was positive for yellow oleander, a known toxin. A hazard statement issued […]

Scranton, Pennsylvania-based Electric City Sweets has recalled 1,644 Red Velvet Milk Chocolate Bars because the product label fails to declare the presence of milk in the ingredient and allergen statement. Individuals who live with an allergy or sensitivity to milk are advised against consuming the […]

New York, New York-based Roland Foods, LLC (“Roland Foods”) has recalled one production code of its 16-ounce Roland® Tahini (100% Ground Sesame Seeds) because the product may contain a trace of Salmonella, reports the FDA. In healthy people, a Salmonella infection may give way to […]

According to the FDA, two lots of H&Natural TejoRoot and H&Natural Brazil Seed Dietary Supplements in 10g pills, as well as two lots of H&Natural Brazil Seed in .167g seeds, have been voluntarily recalled by San Luis, Arizona-based G.A. Mart dba H&Natural. The consumer-level recall […]