794 recalls tagged with “infant product”.
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.
CT New Energy Technology recalls CT-ENERGY nc-02 lithium coin battery chargers sold with four rechargeable 2032 batteries and a USB cable. The recall cites potential for serious injury or death from ingested button cells. Consumers should stop using the charger and contact CT New Energy for a full refund, repair, or replacement kit.
Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.
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 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 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 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 182 MAGNETOM Skyra MRI systems worldwide on August 28, 2025. The recall follows a potential ice blockage in the magnet venting system that could cause a helium leak during a quench. Hospitals should stop using affected devices and follow manufacturer instructions for remediation.
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.
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 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 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 18 MAGNETOM Skyra Fit BioMatrix MRI systems worldwide due to ice blockage in the magnet venting system that could trap helium gas during a quench. The risk is a ruptured helium containment and a potential helium leak into the scanning room. Hospitals and clinicians should stop using the affected devices and await manufacturer instructions.
Chlorpromazine Hydrochloride tablets distributed nationwide by American Health Packaging are recalled after a polyester coil used in packaging showed presence of a micro-organism in a specific lot. No tablets were contaminated. Consumers and healthcare providers should stop using this product immediately and contact Amerisource Health Services LLC for guidance.
Middlefield Original Cheese Cooperative recalled 364.125 cases of shredded Mozzarella/Provolone cheese sold in Ohio, Pennsylvania, Wisconsin, and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact the cooperative for refund or replacement information.
Zydus Lifesciences recall remains active for 270,125 vials distributed across MS, OH, LA and Puerto Rico. The FDA notice cites failed impurities and degradation specifications as the reason. Immediate discontinuation is advised for healthcare providers and patients with ongoing prescriptions. Contact Zydus Pharmaceuticals USA Inc for guidance.
A recall of chlorpromazine hydrochloride tablets is active nationwide in the United States. A specific lot of packaging material to coils used in manufacturing contained a foreign substance with a microorganism detected. Tablets themselves tested negative for microorganisms. Consumers and healthcare providers should stop using the product immediately and contact Amerisource Health Services LLC or
Middlefield Original Cheese Cooperative recalled 364.125 cases of 5 lb shredded mozzarella cheese sold to retailers in Ohio, Pennsylvania, Wisconsin and Texas. The product could be contaminated with Listeria monocytogenes. Consumers should not consume it and should contact the cooperative for refund or replacement.
Middlefield Original Cheese Cooperative recalls 7,455 pounds of Original Swiss Cheese distributed in Ohio, Pennsylvania, Wisconsin and Texas after potential Listeria monocytogenes contamination. The recall affects 5‑lb loaves and 2‑lb deli bags in various packaging. Consumers should not eat this cheese and should contact the cooperative for refund or replacement information.