1,003 recalls tagged with “chemical hazard”.
CA Botana International recalled 1,167 tubes of Doctor. D. Schwab Mineral Sunscreen SPF 50 after CGMP deviations were found. The recall cover identifies lot D54596 with exp 1/31/2028. The distribution includes California, Colorado, Florida, Puerto Rico and Washington.
27,868 blister packs of Sucralfate Tablets, 1 g, distributed nationwide by American Health Packaging are recalled. The recall stems from CGMP deviations that prevent the firm from assuring product identity, strength, quality and purity. Health providers and consumers should stop using the product immediately and await guidance.
USV Private recalled 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%. The product was distributed nationwide in the United States. The defect is failure of impurities/degradation specifications due to an unspecified impurity exceeding the limit. Stop using immediately and contact USV Private Limited or a healthcare provider for guidance.
STAQ Pharma recalled Ketamine Hydrochloride injections distributed nationwide in the United States. The labeling has incorrect or missing lot and expiration date information. Stop using the product and contact STAQ Pharma or your healthcare provider for guidance.
Rong Shing Trading NY Inc recalled Aojia Dried Red Bayberry sold in 5.6-ounce bottles after undeclared sulfites and cyclamates were detected. The recall covers 10 cases distributed to Virginia, New Jersey, Massachusetts and New York. Consumers should not eat the product and should contact Rong Shing Trading NY Inc for a refund or replacement.
Mom Genius recalled retractable safety gates due to entrapment risk that can cause serious injury or death. The recall covers gates with a retractable mesh screen in black and gray. The model is SH.20.006B02. Consumers should stop using the gate and seek a full refund.
YGJT recalled baby loungers sold on SHEIN by YGJT Local Warehouse from June 2025 through August 2025 for $18-$21. The recall cites a safety violation that allows infants to be trapped or fall due to low sides, wide openings at the foot, and no stand. Consumers should stop using the loungers immediately and request a full refund by emailing YGJTrecall@outlook.com.
AstraZeneca recalls 916 Fasenra benralizumab injections distributed nationwide in the United States. The lot is YJ0152 and the NDC is 0310-1730-30. The product is being recalled for lack of sterility assurance. Stop using this product immediately and contact AstraZeneca for guidance.
Viona Pharmaceuticals recalled 13,080 Tavaborole Topical Solution 5%, 10 mL bottles distributed nationwide in the United States. The recall covers Tavaborole Topical Solution 5%, Rx only, manufactured by Zydus Lifesciences Ltd. Discoloration linked to RES #97424 prompted the action. Consumers should stop using the product and contact Viona for guidance.
Sno Pac Foods recalled 4,006 cases of Frozen Organic Spinach sold under Sno Pac Frozen Vegetables and Maika'i Keep Frozen. The spinach may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Sno Pac Foods for refund or replacement.
MG Foods recalls 117 Jumbo Meat Ball Sub sandwiches distributed in Texas and Louisiana. Mozzarella cheese in the product could contain metal shavings. Consumers should not eat the product and should contact MG Foods for refunds or replacements.
Great Lakes Cheese Co recalls 4,131 cases of mozzarella and provolone shredded cheese blends sold under four store brands due to metal fragments from supplier raw material. The hazard involves potential metal fragments detected in the shredded cheese products. Consumers should not consume these products and should contact Great Lakes Cheese Co for refund or replacement information.
Great Lakes Cheese Co Inc recalls 4,298 cases of pizza-style shredded cheese blends sold through retailers nationwide after metal fragments were found in supplier raw material. The defect involves potential metal fragments that could contaminate the cheese. Consumers who may own any of the affected products should not consume them and should contact Great Lakes Cheese Co for refund or replacement.
Advanced Pharmaceutical Technology recalled 22,843 cartons of TESTO-100 CIII testosterone pellets on October 3, 2025. The recall follows a risk of microbial contamination that could compromise product sterility. Consumers and healthcare providers should stop using the product immediately and seek guidance.
Coca-Cola Southwest Beverages LLC recalled 2,322 units of Coca-Cola 12oz Can packs sold in Texas. The products include 24-pack and 35-pack configurations with model numbers 49000012781 / JUN2926MAA and 49000058468 / JUN2926MAA. Consumers should not drink these cans and should contact the company for refunds or replacements.
Food Club recalled 117 cases of Finely Shredded Pizza Style Four Cheese Blend, sold at multiple retailers nationwide, after potential metal fragments were found in a supplier raw material. The 8-ounce packages contain mozzarella, provolone, parmesan and romano cheeses and carry UPC 3680017231. Consumers should not eat this product and should contact Great Lakes Cheese Co for refund or replacement.
In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.
Almpal recalls its dissolved oxygen test kits sold on Amazon after authorities found the sulfuric acid inside the kit lacked required child-resistant packaging. The recall is active as of Oct 2, 2025. Consumers should stop using the kit and follow disposal and refund instructions from the seller.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
Ocean's Kitchen recalled 496 cases of imitation crab meat shredded, distributed in Washington state. The product is refrigerated and vacuum-packaged. The recall cites potential contamination with Clostridium botulinum due to temperature abuse during chilled storage. Consumers should not consume the product and should contact Oceans Kitchen for refunds or replacements.