Recall database
All Product Recalls
- Active recalls
- 4,441
- Current page
- 98
Preema Food Colour Powder Recalled Over Banned Ingredients
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Teva Metoprolol Succinate ER 100 mg Recall Expanded for Failed Dissolution Specifications (2026)
23,568 Medline Surgical Drapes Recalled Over Infection Risk
Ultradent Products Recalls 2,508 Jiffy Original Composite Polisher Cups (Coarse) 12pk (2026)
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
Medline Medcrest Surgical Gowns Recalled 104,004 Units for Delamination Risk (2026)
Why Not Natural Recalls Moringa Capsules Due to Salmonella Risk
Art Monkey LLC recalled 8,500 bottles of Why Not Natural Moringa Capsules on January 28, 2026. The capsules may be contaminated with Salmonella and pose a serious health risk. Consumers should stop using the product immediately and seek refunds.
Koi Koi Trading Recalls Fish Balls Over Allergen Risk
Koi Koi Trading recalled 8,232 cases of frozen fish balls on January 28, 2026. The product contains undeclared wheat and sesame allergens, posing a serious health risk. Consumers should check their freezers and take immediate action.
Koi Koi Trading Recalls Fish Balls Due to Allergen Risk
Koi Koi Trading recalled 344 cases of frozen fish balls on January 28, 2026. The product contains undeclared allergens, wheat and sesame, posing a serious risk to consumers. The recall affects distribution in eight states including California and Texas.
Koi Koi Trading Recalls Fish Balls Due to Undeclared Allergens
Koi Koi Trading recalled 3,884 cases of frozen fish balls on January 28, 2026. The recall was issued due to undeclared allergens, Wheat and Sesame, posing a serious health risk. Consumers should stop using the product immediately and seek a refund.
Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026
Reports of devices sparking/popping and potentially burning patients.
BD 10 mL Luer-Lok Syringe Recalled Over Bundle Packaging Mix-Up in US; 204,000 Units Affected
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Abiomed Impella RP Flex Recall 4,496 Devices Worldwide Over Sensor Drift (2026)
Abiomed recalled 4,496 Impella RP Flex with SmartAssist devices. The recall cites a differential pressure sensor that may malfunction and drift readings. Stop using the device immediately and follow the manufacturer's recall instructions.
Khee Trading Recalls Frozen Oysters Due to Norovirus Risk
Khee Trading Inc. recalled 7,306 cases of Frozen Half Shell Oysters on January 27, 2026. The oysters may be contaminated with Norovirus, posing a serious health risk. Consumers should not consume the product and seek a refund or replacement.
Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Abiomed Impella RP with SmartAssist Recall Affects 291 Units Worldwide in 2026
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Beacon Promotions Recalls M&Ms Over Undeclared Allergens
Beacon Promotions recalled 5,788 units of repackaged M&Ms candies on January 26, 2026. The candies contain undeclared allergens, specifically milk, soy, and peanuts. Consumers should not consume these products and should seek refunds.
Asteria Health Recalls Testosterone Pellets Due to Metal Contamination
Presence of Foreign substance - potential presence of metal particulate matter
Philips Medical Systems Recalls Azurion 3 M12 Due to Hazard
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Philips Medical Systems Recalls Azurion 7 B12 Table Due to Safety Risk
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.