495 recalls tagged with “suffocation risk”.
Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.
GM recalls 2024-2025 Chevrolet Blazer EVs due to a rear parking brake wiring harness that may corrode or become damaged. The defect can cause unintended parking brake activation or loss of function, increasing crash risk. Dealers will inspect and reroute the harness, install anti-abrasive tape, and replace damaged harnesses at no cost. Owner notices mailed October 1, 2025. Contact Chevrolet at 1-[
Quidel recalls 22,470 Rapid Strep A Dipstick tests sold worldwide, including multiple U.S. states. The dipstick test may yield false positive results. Health providers and patients should stop using the device immediately and follow recall instructions. Check with Quidel for refund or replacement options.
Sedecal SA recalled 3 units of the Mobile X-ray system 40KWFXPLUS.004 distributed in California, Illinois and New Jersey after warning users the device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have consequences. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.
Sedecal recalled 7 mobile X-ray systems distributed to California, Illinois and New Jersey after warning that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice highlights potential consequences of improper cleaning. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.
Sedecal SA recalled 6 SM-40HF-B-D-C mobile X-ray systems distributed to consignees in California, Illinois and New Jersey after a notice reminded users the devices are not water-resistant and must be cleaned strictly per the manual. The reminder outlined possible consequences of improper cleaning. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.
Kia America recalls 2025 K5 sedans over a software error in the Power-net Domain Controller that can cause parking lights to flicker. The recall affects 2025 K5 vehicles. Dealers will update the PDC software, or owners can receive an OTA update for free. Letters notifying owners were mailed June 24, 2025. Contact Kia customer service at 1-800-333-4542. Recall SC341.
Volkswagen Group of America recalls 2024-2025 Atlas Cross Sport and Atlas vehicles for rearview camera distortion in reverse. The defect may reduce visibility behind the vehicle and increase crash risk. Dealers will update the camera control unit software free of charge. Owner letters mailed June 5, 2025. Contact VW customer service at 1-800-893-5298.
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.
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.
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.
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.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device SA Angled Punch Awl. The recall covers models 17-5A-AWL3, 17-5A-AWL4, 17-5A-AWL5 with UDI 00843511113056 and 00843511122287/22294. The hazard is failure of fusion system instruments in the field. Consumers should stop use and follow recall instructions.
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.