Browse through 3,495 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
ESR HaloLock wireless power banks, distributed by Waymeet, are recalled. The lithium-ion battery can overheat and ignite, creating a fire and burn hazard. Stop using the recalled power banks and contact Waymeet for a full refund.
AquaStar recalls 22,500 cases of Cocktail Shrimp sold at Walmart and Kroger stores nationwide. The recall warns Cs-137 contamination risk in 6-ounce net weight shrimp products. Consumers should not eat the product and should seek a refund or replacement from AquaStar.
AquaStar recalled 126 cases of Frozen AquaStar Breaded Shrimp sold at Walmart stores nationwide and Kroger banners after Cesium-137 contamination was detected. The product is contaminated with Cs-137. Consumers who purchased the affected shrimp should not eat it and should contact AquaStar via email for refund or replacement.
Empower Brands recalled Remington hair dryers, model D3190DCDN, sold under the Remington brand, due to risk of electrocution if the unit falls into water while plugged in. Consumers should stop using the recalled dryers and contact Empower Brands for a full refund.
Firefly Fuel Inc. recalled Firefly Safe & Green 32 oz. bottles. The recall date is August 14, 2025. The fuel is sold in a clear bottle with a white cap and nozzle applicator. The product label shows Firefly brand, Safe & Green in green font, and claims Non-Toxic and Kosher. The nozzle applicator lacks child-resistant features, violating the Poison Prevention Packaging Act and the Federal Hazardous
Drinkmate recalled certain 1-liter carbonation bottles after receiving reports of potential explosions. Users may suffer serious laceration and hearing damage from exploding bottles. Consumers should stop using the bottles immediately and contact Drinkmate for a free replacement.
Werner recalls 2 ladder models sold nationwide after reports of locking mechanism jams. The recall affects Werner 20' ALMP-20IAA and 24' ALMP-24IAA Multi-Max Pro multi-purpose ladders. Consumers should stop using these ladders and contact Werner for a full refund.
Fresh & Ready Foods recalled 233 Piccolo Pranzo Box sandwiches after undeclared wheat and milk allergens were detected. The product was distributed to 15 California locations. Consumers should not eat the product and should contact Fresh & Ready Foods for refund or replacement information via email.
Fresh & Ready Foods recalled 233 Spanish Club Ciabatta sandwiches sold to 15 California locations after discovering undeclared wheat and milk allergens. The recall is Class I and the hazard is an undisclosed allergen on ready-to-eat sandwiches. Consumers should not eat the sandwiches and should contact Fresh & Ready Foods for refunds or replacements by email.
Beckman Coulter recalled hematology analyzers configured with HGB photometers after reports of erroneously high hemoglobin results in samples with elevated WBC counts. The recall covers DxH 900 systems worldwide. Stop using the device immediately and follow manufacturer instructions. Contact Beckman Coulter or a healthcare provider for guidance.
Philips North America LLC is recalling 181 CT systems worldwide, including Brilliance CT 40 Channel 728235, Brilliance CT 64 Channel 728231, and Ingenuity Flex 728317. The patient support couch may descend to the lowermost position after a replacement. Hospitals and imaging centers should stop using the devices immediately and await recall instructions.
Philips recalled 73 Brilliance CT systems worldwide after determining a ball screw misalignment could cause the patient couch to descend to the lowermost position. The recall covers Brilliance 16 Power, 728240; Brilliance CT 16 Slice, 728246; and Brilliance CT 6 Slice, 728256. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions immediately.
Philips recalled 14 Brilliance iCT SP CT systems, model 728311, sold worldwide including the United States. The patient support couch may descend unexpectedly to the lowermost position because of ball screw misalignment after a replacement. Hospitals should stop using the device immediately and await manufacturer instructions.
Philips recalled 24 CT systems worldwide after finding that the patient support couch may descend unexpectedly following a replacement. The defect involves a misaligned ball screw in the couch mechanism. Hospitals and imaging centers should stop using the device immediately and follow Philips recall instructions.
Philips recalled 285 Ingenuity CT systems worldwide, including 728321, 728323 and 728326 models. A ball screw misalignment after a replacement can cause the patient couch to descend to the lowermost position. Hospitals and clinics should stop using the devices and follow Philips recall instructions.
Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.
Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.
Fresh & Ready Foods recalled 233 units of Chili Crunch Market Mezze sandwiches sold to California private corporate locations. The product contains undeclared wheat, creating a potential severe allergic reaction. Consumers should not consume the product and should contact Fresh & Ready Foods for refund or replacement.
HEB recalled 468 cases of 8oz Blueberry Flavored Yogurt Pretzels distributed in Texas by Dollins Pecan Co, Inc. The product contains undeclared wheat allergen. Consumers should not eat the product and should contact Dollins Pecan Co, Inc via email for refund or replacement.
Philips North America LLC recalled 33 CT systems worldwide after reports of a patient couch descending unexpectedly. The affected models are 728242, 728243, and 728244. Hospitals and clinics should stop using the devices immediately and await recall instructions.