Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Aonic Inc. recalled 3,630 bottles of Aonic Complete Hers dietary supplement on January 15, 2026. Possible contamination with coliforms, E. coli, and Pseudomonas aeruginosa prompted the recall. Consumers in Utah should stop using the product immediately.
Aonic Inc. recalled 780 bottles of its Complete dietary supplement on January 15, 2026, due to potential contamination with E. coli and Pseudomonas aeruginosa. Consumers in Utah should stop using the product immediately and seek refunds or replacements. The recall affects specific lots with expiration dates of December 27, 2026.
KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.
Organic Spices, Inc. recalled 6,288 jars of garlic salt on January 14, 2026. The product contains salt, which is not listed on the label. The recall impacts several states including California and New York.
Organic Spices Inc recalled 980 cases of organic sumac on January 14, 2026. The product contains mislabeled salt, posing a health risk to consumers. The recall affects 11,760 jars distributed across multiple states in the U.S.
Organic Spices recalled 4,692 jars of celery salt on January 14, 2026. The product is mislabeled and contains salt, posing a risk to consumers. The recall affects multiple states including California and Texas.
Gooder Foods recalled 61,176 cartons of pasta on September 10, 2025, due to undeclared allergens. The product may contain cashews, posing a risk to consumers with nut allergies. The affected lots were distributed across multiple states in the U.S. and Canada.
MG Foods-Compass Group recalled 3,099 breakfast burritos on January 13, 2026, due to contamination with small hard plastic fragments. The burritos were distributed across seven states, including Illinois and Ohio. Consumers should not eat the product and seek a refund.
Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.
Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.
McCain Foods USA recalled 67 cases of Sonic Tots on January 12, 2026, after reports of small hard plastic fragments. The frozen potato product weighs 30 lbs per case and is packaged in clear unlabeled poly bags. Consumers should not consume this product and are advised to seek a refund or replacement.
McCain Foods USA Inc. recalled 21,557 cases of Ore-Ida Tater Tots on January 12, 2026, due to contamination with small hard plastic fragments. The affected product was distributed to foodservice accounts across 20 states but not sold in retail stores. Consumers should not consume the product and are advised to seek refunds or replacements.
Ford Motor Company recalled certain 2025 Explorer and Lincoln Aviator vehicles due to a rearview camera software defect. The rearview camera image may fail at speeds of 10 MPH or greater, increasing crash risk. Owners received notification letters on March 28, 2025.
Rising Pharmaceuticals recalled 4,212 bottles of Furosemide Tablets on January 10, 2026. The recall stems from the discovery of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from their healthcare provider.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026. The product may be contaminated with Clostridium botulinum, posing serious health risks. Consumers should not consume the product and seek refunds immediately.
Diva Fam Inc recalled approximately 5.4 million units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and should seek refunds or replacements.
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
Diva Fam Inc recalled 5.4 million jars of Sea Moss Gel on January 9, 2026. The recall follows concerns of potential Clostridium botulinum contamination. Consumers should stop using the product immediately.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume this product and should seek refunds or replacements immediately.