Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Siemens Medical Solutions USA recalled 182 MRI machines on August 28, 2025, due to a risk of helium leaks. An ice blockage in the magnet venting system could cause pressure build-up, leading to a potential rupture. Users must stop using the device and follow recall instructions immediately.
Siemens Medical Solutions USA recalled nine MRI scanners on August 28, 2025. The devices may develop ice blockages in the venting system, risking helium leaks. Healthcare providers must stop using the scanners immediately.
Siemens Medical Solutions USA recalled 39 MAGNETOM Prisma MRI scanners on August 28, 2025, due to a potential helium leak hazard. The recall affects units distributed worldwide, with a significant risk of helium gas build-up within the containment system. Healthcare providers must stop using the device immediately and follow recall instructions.
Siemens Medical Solutions USA recalled 30 units of the MAGNETOM Skyra fit MRI system on August 28, 2025. The recall addresses a potential ice blockage in the magnet venting system that could lead to a helium leak. The device is distributed worldwide, including the US and multiple countries.
Siemens Medical Solutions USA recalled one BIOGRAPH One MRI system on August 28, 2025. The recall affects model number 11689172 due to a potential helium leak risk. Patients and healthcare providers must stop using the device immediately and follow the manufacturer’s instructions.
Siemens Medical Solutions USA recalled 46 MAGNETOM Verio Dot systems on August 28, 2025. The recall stems from a risk of ice blockage in the magnet venting system. This could lead to a helium leak, posing serious safety hazards.
Siemens Medical Solutions USA recalled 23 units of the Biograph mMR on August 28, 2025, due to a potential helium leak risk. The recall affects devices distributed worldwide, including the US. This Class I recall poses a high hazard to patients and healthcare providers.
American Health Packaging recalled 1,062 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the detection of a micro-organism in auxiliary packaging materials. No micro-organism was found on the tablets themselves, but consumers should stop using the product immediately.
Middlefield Original Cheese Cooperative recalled 7,455 pounds of shredded mozzarella cheese on August 27, 2025. The product may contain Listeria monocytogenes, which can cause serious illness. Consumers should not consume the cheese and seek refunds or replacements.
Unichem Pharmaceuticals recalled 230 bottles of Cyclobenzaprine Hydrochloride Tablets on August 27, 2025. The recall stems from a labeling mix-up with Meloxicam tablets, which could lead to serious health risks. Consumers should stop using the product immediately and contact their healthcare provider.
American Health Packaging recalled 2,708 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall follows the detection of a micro-organism in product packaging, though no contamination was found on the tablets themselves.
American Health Packaging recalled 1,757 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the detection of a microorganism in packaging materials, though no contamination was found on the tablets themselves. Consumers should stop using the product immediately and contact healthcare providers for guidance.
American Health Packaging recalled 873 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the presence of a micro-organism in packaging material. No micro-organisms were found on the tablets themselves.
Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar on August 27, 2025. The cheese may be contaminated with Listeria monocytogenes, posing a high health risk. Consumers in Ohio, Pennsylvania, Wisconsin, and Texas should not consume the product.
Middlefield Original Cheese Co-op recalled 364 cases of Monterey Jack and Provolone cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers should not consume the affected products and should seek a refund or replacement.
Middlefield Original Cheese Cooperative recalled 364 cases of cheddar cheese on August 27, 2025. The products may contain Listeria monocytogenes, a harmful bacteria. Consumers should avoid eating the cheese and seek refunds or replacements.
Sunrise Creamery recalled 364 cases of Dilly Pickle Monterey Jack Cheese on August 27, 2025. The product may contain Listeria monocytogenes, posing a serious health risk. Consumers should avoid eating this cheese and seek refunds immediately.
Middlefield Original Cheese Co-op recalled 364 cases of Organic Gouda Cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes, which can cause serious illness. Consumers should not eat the cheese and seek refunds or replacements.
Middlefield Original Cheese Cooperative recalled 364 cases of Swiss cheese on August 27, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not consume the product and seek refunds immediately.
Middlefield Original Cheese Cooperative recalled 364 cases of shredded mozzarella/provolone cheese on August 27, 2025, due to potential Listeria contamination. This recall affects 7,455 pounds of cheese distributed in Ohio, Pennsylvania, Wisconsin, and Texas. Consumers should not eat the product and seek refunds or replacements immediately.