1,003 recalls tagged with “chemical hazard”.
Taro Pharmaceuticals recalled Clindamycin Phosphate USP, 1% topical solution on November 26, 2025. The recall affects specific lots due to failed impurity testing. Consumers should stop using the product immediately and consult healthcare providers.
Ferndale Laboratories recalled 24,589 vials of Mastisol Liquid Adhesive due to a defect. The butyrate tube may crack during use, making the product unusable. The recall affects products distributed in the U.S. and the U.K., announced on November 25, 2025.
Imu-Tek Animal Health recalled 113 bottles of Immuno-5 Colostrum Powder on November 25, 2025. The product contains an undeclared milk allergen, posing a risk to consumers with milk allergies. The recall affects states including CA, TX, and FL.
Prairie Farms Dairy recalled 3,752 gallons of Fat Free Milk on November 25, 2025. The milk may contain food-grade cleaning agents, posing a health risk. Consumers should not consume the product and seek refunds or replacements.
Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.
Gimme Coffee, Inc. recalled 252 boxes of Decaf de Agua coffee pods on November 24, 2025. The product contains undeclared caffeine, posing a risk to consumers sensitive to caffeine. Affected products include those with best-by dates of September 30, 2025, and October 15, 2025.
Bell Industries recalled 66 units of Zen Cleanse Blend herbal tea on November 24, 2025. The recall follows potential Salmonella contamination. The product was distributed to three customers in Massachusetts, Texas, and Wisconsin, but did not reach retail shelves.
Breckenridge Pharmaceutical, Inc. recalled 7,389 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations and the presence of N-nitroso-duloxetine impurity above FDA limits. Consumers should stop using the product immediately and contact healthcare providers for guidance.
Draeger, Inc. recalled 431 units of the Vapor 2000 anesthetic vaporizer on November 24, 2025. A component of the devices contained impurities and did not meet specifications, posing a high hazard risk. Healthcare providers and patients should cease use immediately and follow recall instructions.
Towa Pharmaceuticals recalled 3,397 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations resulting in N-nitroso-duloxetine levels exceeding FDA limits. Consumers must stop using the product immediately.
Changchun Wancheng Bio-Electron Co. recalled 3,300 Vivoo test strips on November 22, 2025. The devices may provide inaccurate results, leading to inappropriate medical actions. Affected products include sodium, Vitamin C, and hydration tests.
Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.
LotFancy recalled 91,366 urinary tract infection test strips on November 22, 2025. The strips may produce false results, risking inappropriate medical intervention. Affected products include various models sold nationwide in states like Texas, Georgia, and California.
Changchun Wancheng Bio-Electron Co. recalled 500 Vivoo Protein Test strips on November 22, 2025. The devices may provide false diagnostic results, leading to inappropriate medical interventions. This recall affects consumers nationwide in Texas, Georgia, and California.
Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.
Changchun Wancheng Bio-Electron Co. recalled 500 Vivoo pH Test strips on November 22, 2025. The recall follows concerns over false diagnostic results that could lead to inappropriate medical interventions. These devices were distributed nationwide, including Texas, Georgia, and California.
Changchun Wancheng Bio-Electron Co. recalled 4,800 Exploro Male Fertility Tests on November 22, 2025. These devices may provide false diagnostic results, potentially leading to inappropriate medical interventions. Consumers should stop using the product immediately and follow recall instructions.
SB FOOD recalled 100 cases of Yoyo Gummy Tropical Flavor on November 21, 2025. The products contain an unallowed color, Carmoisine (E122), posing health risks. Consumers in 14 states should stop consuming the product immediately.
SB FOOD recalled 100 cases of Yoyo Gummy Assorted Flavor on November 21, 2025. The product contains an unapproved color, Carmoisine (E122), posing health risks. Consumers should not consume the candy and seek refunds.
Ambriola Co., Inc. recalled 184 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria that can cause serious illness. Consumers in multiple states should not consume this product.