Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Viewrail recalled electronic LED modules on August 14, 2025, due to a fire hazard. The model "E2-WR" can overheat and melt, posing risks to consumers. Affected modules were sold from August 2023 through June 2025 for about $80.
Synergy Housewares recalled Wolfgang Puck petite tea kettles on August 14, 2025, due to a burn hazard. The kettle's infuser basket lid can detach during use, posing serious risks. About 20,000 units sold from August 2020 through January 2025 are affected.
ESR recalled HaloLock wireless power banks on August 14, 2025, following reports of fire hazards. The lithium-ion batteries can overheat and ignite. Consumers should stop using these devices immediately and return them for a full refund.
STWUQIKONG recalled children's tower toys on August 14, 2025, due to a choking hazard. The toys contain small balls and violate the small ball ban, posing risks to children under three years. Consumers must stop using the toys immediately and return them for a full refund.
Empower Brands recalled Remington hair dryers on August 14, 2025, due to electrocution risks. The D3190DCDN model lacks immersion protection, posing a danger if dropped in water. Consumers should stop using the product immediately.
Werner recalled 20,000 Multi-Max Pro ladders on August 14, 2025 after reports of locking mechanism failures. The recall affects models ALMP-20IAA and ALMP-24IAA sold in silver with blue features. Consumers must stop using the ladders and contact Werner for a refund.
Drinkmate recalled certain 1-liter carbonation bottles on August 14, 2025. The bottles can explode, posing serious impact and laceration hazards. Consumers should stop using the bottles and contact Drinkmate for a free replacement.
Philips recalled 181 CT scanner units on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728235, 728231, and 728317 distributed worldwide. Healthcare providers and patients must stop using these devices immediately to ensure safety.
Fresh & Ready Foods LLC recalled 233 units of Tuscan Artichoke and Mozzarella Salad on August 13, 2025. The recall stems from undeclared wheat and milk allergens in ready-to-eat sandwiches. The affected products were distributed to 15 locations in California.
Fresh & Ready Foods LLC recalled 233 units of Piccolo Pranzo Box sandwiches on August 13, 2025. The recall follows the discovery of undeclared allergens, specifically wheat and milk, posing a serious risk to consumers. The recalled products were distributed to 15 locations across California.
Sandoz, Inc. recalled 1,680 bottles of Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension on August 13, 2025. The recall stems from temperature abuse that may compromise the product's efficacy. Consumers should stop using the product immediately and contact their healthcare provider or Sandoz for guidance.
Fresh & Ready Foods LLC recalled 233 units of Spanish Club Ciabatta sandwiches on August 13, 2025. The recall stems from undeclared allergens, specifically wheat and milk, posing a high risk to consumers. The products were available at 15 corporate locations across California.
Philips recalled 81 IQon Spectral CT systems on August 13, 2025, due to a potential fall hazard. The patient support table may descend unexpectedly due to a ball screw misalignment. Healthcare providers and patients must stop using the device immediately.
Philips recalled 285 CT systems on August 13, 2025, due to a risk of patient support tables descending unexpectedly. The recall affects model numbers 728321, 728323, and 728326. Users should stop using the devices immediately and follow manufacturer instructions.
Fresh & Ready Foods recalled 233 units of ready to eat sandwiches on August 13, 2025. The recall stems from undeclared wheat allergens that pose a serious risk to consumers. The sandwiches were distributed to 15 corporate locations in California.
Beckman Coulter recalled the UniCel DxH 900 COULTER Cellular Analysis System on August 13, 2025, due to erroneous high hemoglobin results. The devices may misreport hemoglobin levels on samples with elevated white blood cell counts. This recall affects devices distributed worldwide, including the U.S.
HEB recalled 468 cases of Blueberry Flavored Yogurt Pretzels on August 13, 2025. The recall affects 8oz packages with UPC code 9787011400 due to undeclared wheat allergen. Consumers should stop consuming the product immediately.
Philips recalled 73 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728240, 728246, and 728256 distributed worldwide. This recall includes systems sold across the US and several countries globally.
Beckman Coulter recalled the UniCel DxH 600 Cellular Analysis System on August 13, 2025. The devices may produce erroneously high hemoglobin results in patients with elevated white blood cell counts. This recall affects medical facilities worldwide, including the United States.
Philips recalled 33 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. A misalignment in the ball screw can cause the couch to drop to its lowest position. The recall affects models distributed worldwide, including the U.S. and numerous countries.