These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
EcoFlow Technology recalled Delta Max 2000 Power Stations due to a fire hazard. The recall affects model EFD310, identified by a black and silver design. Consumers should stop using the product immediately and seek a firmware update for repair.
Glycar SA Pty. recalled 18 units of the SJM Pericardial Patch on October 9, 2025. The affected lot may not meet required tensile strength specifications. Healthcare providers and patients should stop using this device immediately.
Mom Genius recalled Retractable Safety Gates on October 9, 2025, due to a risk of serious injury or death. The gates violate mandatory safety standards and pose an entrapment hazard. Consumers should stop using the gates immediately and seek a refund.
Taoscare recalled 3 boxes of motion sickness patches on October 9, 2025. The product was marketed without an approved NDA/ANDA. Consumers should stop using the patches immediately and seek guidance.
Pivotal Health Solutions recalled 34 heated massage tables on October 9, 2025. The heat function may overheat, posing a risk of smoldering and melting. Affected units are distributed nationwide in the U.S., Canada, and Japan.
Waymeet expanded its recall of ESR HaloLock wireless power banks on October 9, 2025. The models 2G505, 2G520, 2G505B, and 2G512B pose serious burn and fire hazards. Consumers must stop using these devices immediately and return them for a full refund.
STAQ Pharma Inc. recalled Ketamine Hydrochloride 50mg/5 mL syringes on October 9, 2025. The recall affects products with incorrect or missing lot and expiration dates. The FDA classified this recall as Class III due to potential risks to patient safety.
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.
AstraZeneca recalled 916 pre-filled syringes of Fasenra on October 8, 2025. The recall follows a lack of assurance of sterility, posing serious health risks. Consumers and healthcare providers must stop using the product immediately.
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.
Rising Pharma Holdings recalled 2,064 bottles of Carbidopa, Levodopa, Entacapone tablets on October 7, 2025. The recall followed reports that bottles contained incorrect dosages. The affected product poses a high risk due to potential overdose.
Del Mar Food Products recalled 966 cases of organic IQF chopped spinach on October 7, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers should not eat the product and can seek a refund.
Nutrition for Longevity recalled 635 units of Loaded Veggie Grain Bowl on October 7, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers in ten states should not consume the product and seek refunds.
Sno Pac Foods recalled 4,006 cases of frozen organic spinach on October 6, 2025, due to potential Listeria contamination. Affected products include various lot codes with best-by dates ranging from April to July 2027. Consumers should not eat this product and seek refunds immediately.
Zydus Lifesciences recalled 13,080 bottles of Tavaborole topical solution on October 6, 2025, due to discoloration. The recall affects products distributed nationwide in the USA. Consumers must stop using the product immediately and contact their healthcare providers for guidance.
Volkswagen recalled certain 2025 ID. Buzz vehicles on October 4, 2025. The brake system warning light may display incorrect symbols and colors. This defect increases the risk of a crash.
MG Foods recalled 117 units of Jumbo Meat Ball Sub on October 4, 2025. The recall stems from potential metal shavings in the mozzarella cheese. Consumers in Texas and Louisiana should not consume the product and seek a refund.
Coca-Cola Southwest Beverages recalled 1,115 units of Coca-Cola Zero Sugar 12oz cans on October 3, 2025. The recall stems from potential metal contamination in the product. Consumers should not consume the affected cans and seek refunds.
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.
Good & Gather recalled 1,850 cases of Mozzarella & Parmesan shredded cheese on October 3, 2025. The recall stems from potential metal fragments found in the product. Consumers should not consume the cheese and seek a refund or replacement.