250 recalls tagged with “fire hazard”.
Zydus Pharmaceuticals USA Inc. recalls 4,344 bottles of Entecavir tablets nationwide over impurity/degradation specification failures. The product, Entecavir Tablets, 0.5 mg, carries NDC 68382-920-06 and Lot E309376 with Exp 11/30/2025. The recall is active as of Sept. 24, 2025.
Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalls 300 units of the Allura Xper FD20/15 with model 722058 after the BIOS battery may deplete prematurely, causing startup failure. The recall covers worldwide distribution. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Fagron Compounding Services recalls 109,320 sterile single-dose bevacizumab syringes nationwide due to lack of assurance of sterility. Healthcare providers and patients should stop using the product immediately. Contact Fagron Compounding Services or a healthcare provider for guidance. The recall was issued on 2025-08-29 and remains active as of 2025-09-24.
Northeast Scientific recalled 165 units of the NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter sold nationwide in the United States. The recall cites the potential breach of sterile barrier packaging that could compromise sterility. The device is not cleared for marketing in the U.S. and has a high-risk hazard designation. Patients and healthcare providers should stop using the产品,
Getinge Disinfection Ab recalled 788 units of the 88-Series Washer-Disinfector worldwide, including US states Colorado, Massachusetts, New Mexico and New Hampshire. The device can overheat if circulation pressure calibration is not performed or performed incorrectly and the low-pressure alarm fails to trigger. Manufacturers advise stopping use and following recall instructions.
Air Vent recalled electric motors used in gable- and roof-mounted attic fans sold from August 2003 through December 2013. The recall covers five model numbers and centers on a safety cutoff that may short and ignite. Owners should stop using recalled motors and contact Air Vent for a full refund.
Granules Pharmaceuticals recalled 9,917 bottles of mixed-salts amphetamine extended-release capsules nationwide. The recall was issued August 28, 2025 and remains active. The FDA cited failed impurities/degradation specifications as the reason. Healthcare providers and consumers should stop using the product immediately and contact Granules Pharmaceuticals for guidance.
DT Swiss recalled carbon road wheels sold aftermarket and on high-end bikes due to a wheel integrity defect that can cause a crash. The recall covers wheels with DT Swiss ID codes of 2740000 or higher. DT Swiss provided a replacement remedy. Consumers should stop riding recalled wheels and contact DT Swiss for a replacement.
Siemens Medical Solutions USA recalls 69 MAGNETOM Verio MRIs worldwide after an ice blockage could trap helium gas during a quench. A rupture of the helium containment system may leak helium into the scanning room. The recall affects models with number 10276755 and serials including 40649 and others. Patients and providers should stop using the device and follow manufacturer instructions.
Siemens Medical Solutions USA recalled 9 MAGNETOM Cima.X MRI systems worldwide. A potential ice blockage in the magnet venting system could prevent helium from escaping during a quench, risking rupture and a helium leak into the scanning room. Hospitals and healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.
Siemens Medical Solutions USA recalled 23 Biograph mMR PET-MRI systems worldwide after detecting an ice blockage in the magnet venting system. In a magnet quench, helium gas may not escape through vent paths, risking rupture of the helium containment and a leak into the scanning room. Hospitals and providers must stop using the device immediately and follow the manufacturer’s recall instructions.
Siemens Medical Solutions USA recalled 46 MAGNETOM Verio Dot Upgrade MRI systems sold to hospitals worldwide after an ice blockage could prevent venting during a quench. The blockage could cause pressure to build in the helium containment system, potentially rupturing it and releasing helium into the scanning room. Hospitals and providers should stop using the device immediately and follow Siemens
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA recalls MAGNETOM Spectra MRI with Model Number 10655588 after possible ice blockage in the magnet venting system could cause a helium leak during a quench. The recall covers worldwide distribution including the United States. Patients should stop using the device and follow manufacturer instructions for recall procedures.
Siemens Medical Solutions USA issued a global recall for the MAGNETOM Connectom.X MRI system, Model 11371480. One unit is affected. A potential ice blockage in the magnet venting system could cause a helium leak during a quench. Users should stop using the device and await manufacturer instructions.
Hyundai Motor America is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts may have been improperly tightened, which can cause a loss of drive power and engine damage, potentially resulting in an oil leak. Owner notification letters are expected to be mailed October 24, 2025, and dealers will replace the engine free of charge.
Ford is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles because the instrument panel may fail at startup. The recall covers 2025-2026 models. Ford will provide an IPC software update via dealer service or OTA at no cost. Owner letters were mailed September 5, 2025. Contact Ford customer service at 1-866-436-7332. Recall number 25S88.
CooperVision recalled 4,140 MyDay Toric contact lenses sold nationwide in the United States. The recall cites an invalid sterilization cycle for one lot. Patients should stop wearing the lenses and consult their eye care providers for guidance.
IBC Technologies recalled CX Series Combi Boilers for burn hazards. The recall covers CX-199 and CX-150 models with specific serial ranges. Consumers should stop using recalled boilers immediately and contact IBC for a free in-home repair to install a mixing valve.