Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Ventura Foods recalled 379 cases of its peanut butter and strawberry jam duo on April 30, 2025. Pieces of blue plastic were found in the product during production. Consumers should not eat the product and should seek a refund.
Turkana Food Inc. recalled 352 cases of Floria Dried Apricots, 200-gram packages, distributed to retailers in 19 states. The recall was issued on April 29, 2025. The product contains undeclared sulfites. Consumers should not eat it and should contact Turkana Food Inc. for refund or replacement via email.
3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets due to incorrect flow rates and outlet temperature locations. This defect can affect the warming of fluids, posing serious risks to patients. Healthcare providers must stop using these devices immediately and follow the manufacturer’s instructions for returns.
Ford recalls 2024-2025 F-150 and Expedition and 2024 Navigator SUVs due to a misaligned engine cup plug that can cause a rapid oil leak. The leak may stall the engine and, if oil contacts hot parts, can ignite a fire. Ford says dealers will inspect and replace the plug at no charge; owner letters were mailed May 22, 2025.
Honda recalled 2024-2025 ADV160 scooters after discovering the oil pump driven gear may fail, causing a loss of drive power. The loss of drive power could lead to a crash. Owner letters were mailed August 6, 2025, and dealers will replace the gear free of charge under recall KR9.
Sanders Candy Factory recalled 5,020 pounds of bulk almonds on March 25, 2025. Elevated levels of aflatoxin prompted the recall. The product was distributed to one customer and not sold to consumers.
Chrysler recalls 2025 Jeep Wagoneer S BEVs after headlight aim adjustments fail to meet FMVSS 108. Dealers will correct by adjusting plugs at no charge. Letters to owners began April 3, 2025. No injuries reported in the notice.
ESAOTE recalled 5 Endocavity Ultrasonic Probe E 3-12 units sold in the United States to healthcare providers in NC and TX. A potential weakness in the probe body could cause liquid to leak from the terminal part of the casing near the cable. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.
AUDI Q4 E-Tron and ID.4 models are recalled by Volkswagen Group of America for a faulty on-board charger that may stop charging the 12-volt system. The recall affects 2024-2025 models. Dealers will replace the on-board charger free of charge. Letters notifying owners were mailed May 20, 2025.
Kia America, Inc. recalls 2025 EV9 vehicles for a damaged rear gear drive unit shaft from improper welds. The defect can cause loss of drive power and raise crash risk. Kia asks owners to contact dealers for a free replacement and lists SC337 as the recall number.
BMW recalls 2025 X3 30 xDrive vehicles due to an overheated positive battery cable connection that can cause engine stall and fire risk. The recall affects 2025 X3 models and affects owners nationwide. Dealers will inspect and tighten or replace the positive battery cable and starter-generator at no charge. Letters to owners were mailed June 5, 2025.
World Perfumes Inc. recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic in Florida after broken or leaking containers were reported. The recall covers iodine 2% antiseptic distributed by Essential Products. Consumers should stop use immediately and contact World Perfumes or a healthcare provider for guidance.
MEDITECH released an active recall for the Expanse Laboratory calculator/data processing module. The recall covers 148 units distributed worldwide, including the US, UK, Canada, Ireland and the British Virgin Islands. The hazard concerns simultaneous multi-key inputs potentially removing data from the first field in screens or questionnaires.
Honda recalled 2025 Pilot SUVs and related Acura MDX Type-S and TLX Type-S vehicles sold through Honda and Acura dealer networks after a FI-ECU software error may cause engine stall or a loss of power. Dealers will reprogram the FI-ECU at no charge. Owner letters were mailed March 17, 2025. Contact Honda customer service at 1-888-234-2138 for recall EL1 and AL0. For updates, use the NHTSA hotline
Subaru of America, Inc. is recalling certain 2025 Forester vehicles equipped with 18-inch aluminum alloy wheels. The lug seat surface may be incorrectly specified, which can cause the wheel to detach and reduce vehicle stability. Owner notification letters were mailed February 28, 2025, and dealers will inspect and replace the wheels as necessary at no charge.
CorNeat Vision recalled EverPatch surgical matrix (REF 1036295) in a worldwide distribution that includes 50 states and several countries. The recall addresses retroactive labeling corrections to include prevention and management of would dehiscence. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.
Olympus Corporation of the Americas recalled 633 units of the Cystoscope Outer Sheath, Model WA22810A on September 13, 2024. The recall occurred due to potential device damage when used with a GreenLight Laser for BPH therapy. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Intuitive Surgical recalled 144 units of the da Vinci 5 Surgeon Console Column Motor Connector on August 21, 2024. Users reported a potential ergonomic lock issue that could delay or abort surgical procedures. Healthcare providers must stop using the devices immediately and follow the recall instructions.
Mothers' Milk Bank of Alabama recalled 25 bottles of pasteurized donor human milk on August 18, 2024. The recall follows concerns about potential physical contaminants. Consumers in Alabama should not consume this product and should seek refunds or replacements.
Omnia Medical issued a recall for 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device and TiBrid SA Angled Screwdrivers after field failures were reported. The recall covers nationwide distribution in AZ, CA, NJ, NV, OK and WA. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.