Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
CHETAK NEW YORK recalled 5,232 packets of Deep Sprouted Mat on June 28, 2025. The product tested positive for Salmonella, a serious health risk. Consumers in CA, NJ, IL, FL, and TX should not consume the product and seek refunds.
bioMerieux recalled 235,269 VITEK 2 Gram-negative AST Test Kits on June 26, 2025. The recall follows potential false resistant results for Colistin with specific bacteria. This may affect patient treatment decisions in multiple countries.
BulkSupplements.com recalled 1,001 units of Inositol powder on June 25, 2025, due to potential contamination with Staphylococcus aureus. The recalled products include 250g, 500g, and 1kg packages sold in the U.S. and several international locations.
Orthofix U.S. recalled three intervertebral body fusion devices on June 24, 2025. A labeling error states the width as 33 mm instead of the correct 37 mm. Patients and healthcare providers must stop using the device immediately.
Nirwana Foods recalled its Golden Raisin product on June 23, 2025, due to undeclared sulfites. This recall affects bags sold in New Jersey and New York. Consumers should not consume the product and seek a refund.
Quidel Corporation recalled 22,470 Dipstick Strep A Tests on June 17, 2025, due to potential false positive results. The recall affects tests distributed in multiple U.S. states and internationally. Patients and healthcare providers must stop using the device immediately.
Cheesecake Royale recalled 2,880 pecan bars on June 17, 2025, due to mislabeling of allergens. The affected bars were distributed in Texas. Consumers should not consume the product and seek refunds immediately.
Black Girl Vitamins recalled 9,657 bottles of its B12 dietary supplement on June 13, 2025. The product contains undeclared peanuts, which poses a serious risk to individuals with peanut allergies. Consumers should stop using the product immediately and seek a refund.
Immunocore Limited recalled 7,572 vials of KIMMTRAK injection on June 10, 2025. The affected lots may not provide the intended therapeutic effect. Consumers and healthcare providers should stop using the product immediately.
SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, due to improper cleaning instructions. The device is not water-resistant, posing a potential hazard for users. This recall serves as a reminder to follow all cleaning protocols strictly to avoid consequences.
SEDECAL SA recalled eight mobile X-ray systems on June 10, 2025. The recall follows warnings that the devices are not water-resistant and must be cleaned per the manual. Users must stop using the device immediately to avoid potential injuries.
SEDECAL SA recalled four units of its Mobile X-ray system on June 10, 2025, due to water-resistance issues. Improper cleaning can lead to serious safety hazards. Users must stop using the product immediately and follow recall instructions.
SEDECAL SA recalled one unit of its SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The device poses a high hazard as it is not water-resistant and can lead to improper cleaning issues. Users must stop using the equipment immediately and follow the recall instructions sent via email.
Sedecal recalled 24 units of its Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The equipment is not water-resistant and can lead to safety issues if not cleaned according to the manual. Healthcare providers and patients must stop using the device immediately.
SEDECAL SA recalled 1,198 units of its MobileDiagnost wDR 2.2 X-ray system on June 10, 2025. The equipment is not water-resistant and may pose hazards if not cleaned according to the manual. Users must stop using the device immediately and contact the manufacturer for further instructions.
SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, due to a lack of water resistance. Improper cleaning can lead to serious hazards. Users must stop using the device immediately and follow the manufacturer’s instructions.
Sedecal recalled six units of its mobile X-ray system on June 10, 2025. Users must stop using the device due to a risk of malfunction if not cleaned properly. The equipment is not water-resistant, which may lead to safety hazards.
Sedecal recalled 27 units of its Mobile X-ray system on June 10, 2025. The devices lack water resistance and require strict cleaning per the manual. Improper cleaning could lead to serious issues for users.
Sedecal recalled 39 units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and may pose a hazard if improperly cleaned. Users must follow specific cleaning instructions to avoid potential risks.
SEDECAL SA recalled its Mobile X-ray system on June 10, 2025, due to cleaning safety concerns. The device is not water-resistant and improper cleaning may lead to serious consequences. Healthcare providers and patients must stop using the device immediately and follow recall instructions.