Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
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
Viewrail recalls the electronic LED module E2-WR used with floating stairs and rails after a fire hazard was identified. The recall covers modules located inside the metal stringer tube at the back of the stairs. The recall was announced by the CPSC on 2025-08-14. Consumers should stop using the module and contact Viewrail for a replacement or refund.
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.
STWUQIKONG recalled a three-tier spiral tower toy sold on Shein because of a choking hazard. The recall was announced on August 14, 2025. The toy includes three yellow balls and is designed for children under three, violating the small-ball ban. Stop using the product immediately and email STWUQIKONG_RECALL@hotmail.com to receive a full refund.
Synergy Housewares recalls Wolfgang Puck Petite Tea Kettles sold on HSN for a burn hazard. The recall covers 14 oz stainless-steel kettles with a removable infuser basket. The infuser lid can detach during use. Consumers should stop using the kettle and seek a free lid replacement or repair from Synergy Housewares.
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.
Philips North America recalls 210 CT systems worldwide after reports that the patient support couch may descend unexpectedly to the lowest position following a replacement. Philips issued a recall dated 2025-08-13 with active status. The recall number is Z-2598-2025. Stop using immediately and follow manufacturer instructions.
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.
Philips North America has issued a recall for 81 IQon Spectral CT systems, Model 728332, sold worldwide. The patient support table may descend unexpectedly to the lowest position due to ball screw misalignment after a replacement. Stop using the device immediately and follow manufacturer 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.
Novartis Manufacturing NV and Sandoz Inc recall ciprofloxacin 0.3% and dexamethasone 0.1% otic suspension after temperature abuse. The recall affects one consignee in California. Consumers and health care providers should stop using the product immediately and follow guidance from Sandoz or a healthcare provider.
Beckman Coulter recalled the UniCel DxH 600 COULTER Hematology Analyzer configured with an LED HGB Photometer, distributed to laboratories worldwide. The device may produce erroneously high hemoglobin results when WBC counts are elevated. Labs and healthcare providers should stop using the device immediately and follow Beckman Coulter's recall instructions.
Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System configured with the LED HGB Photometer REF C34520. The hematology analyzer may produce erroneously high hemoglobin results on samples with elevated white blood cell counts. Labs should stop using the device immediately and follow Beckman Coulter's recall instructions.
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.
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.
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.
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.