Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
EcoFlow Technology recalled Delta Max 2000 Model EFD310 portable power stations. The units may overheat and ignite, posing a burn and fire risk. Consumers should stop using the recalled power stations and follow EcoFlow’s instructions to install a firmware update for repair.
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.
Bellabu Bear recalls its bamboo sherpa children's robes sold at Saks Fifth Avenue stores and online retailers from January 2024 through July 2025 for about $60. The robes do not meet mandatory flammability standards for children's sleepwear and pose a burn risk. Stop using the recalled robes and contact Bellabu Bear for a full refund or store credit.
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.
Pivotal Health Solutions is recalling 34 Quantum Q400 intersegmental heated massage tables sold nationwide in the United States, Canada and Japan. The recall cites heat-function components that can be damaged over time when pressed, risking overheating, smoldering and melting of the vinyl cushion. Clinicians and patients should stop using the device immediately and await manufacturer instructions.
Glycar SA recalls 18 SJM Pericardial Patch with EnCap Technology 5x10 cm distributed in the US to healthcare facilities. The lot may not meet the required tensile strength specification. Stop use and follow manufacturer instructions provided by Glycar and your healthcare provider. Notification was issued by email.
C-RAD POSITIONING AB recalled 189 Catalyst and Catalyst+ devices on October 9, 2025, due to issues with stereotactic radiosurgery (SRS) treatment. The defect may lead to incorrect patient positioning, potentially compromising treatment effectiveness. The recall affects devices distributed across 37 countries, including the United States.
Sprouts Farmers Market recalled 4,896 units of Smoked Mozzarella Pasta Salad on October 8, 2025. The salad may contain Listeria monocytogenes, a serious pathogen. Consumers should not eat the product and seek refunds immediately.
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.
Del Mar Food Products Corp. recalls 966 cases of Organic IQF Chopped Spinach 35 lbs sold in the United States, including Minnesota distribution. The product may be contaminated with Listeria monocytogenes. Consumers who purchased the spinach should not eat it and should contact Del Mar Food Products for refund or replacement.
Rising Pharma Holdings recalled 2,064 bottles of Carbidopa, Levodopa and Entacapone tablets distributed nationwide in the United States. Sealed bottles labeled 25 mg/100 mg/200 mg contained 37.5 mg/150 mg/200 mg instead. Healthcare providers and patients should stop using immediately and await recall letter guidance.
Nutrition for Longevity recalled 635 Loaded Veggie Grain Bowls shipped directly to consumers in 11 states after a potential Listeria monocytogenes contamination was identified. The recall involves a 309 g ready-to-eat veggie bowl with N4L code V3FR and model 25254. Consumers should stop using the product and contact Nutrition for Longevity for refund or replacement.
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.
Volkswagen Group of America recalls 2025 ID. Buzz vehicles due to an incorrect brake warning light symbol and color on the instrument panel. Dealers will update the instrument panel software at no charge. Letters notifying owners were mailed June 6, 2025. Contact VW at 1-800-893-5298 for recall 90A2.
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.
Target recalls 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend sold at Target stores after metal fragments were found in a supplier ingredient. The issue involves potential metal fragments from a supplier raw material. Consumers should not consume this product 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.