Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Evergreen Orchard Farm recalled 197 cases of Jujube Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The juice was distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds immediately.
North American Rescue recalled 552 Junctional Emergency Treatment Tools on July 1, 2025. The device may have a manufacturing defect that compromises its structural integrity. Healthcare providers should stop using it immediately and follow recall instructions.
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.
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.
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.
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 unit of its Model SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The recall follows concerns that improper cleaning may lead to equipment failure. Users in California, Illinois, and New Jersey received an email warning regarding the device's lack of water resistance.
SEDECAL SA recalled six units of its Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The equipment is not water-resistant, posing a potential hazard if not maintained according to the manual. Users must stop using the device immediately and follow recall instructions.
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 recalled nine units of its SM-40HF-Batt Mobile X-ray system on June 10, 2025, due to safety concerns. The equipment is not water-resistant and improper cleaning could lead to dangerous consequences. Patients and healthcare providers must stop using the device immediately.
SEDECAL SA recalled three Mobile X-ray systems on June 10, 2025, due to water resistance concerns. Users must strictly adhere to cleaning instructions to prevent potential hazards. The recall affects units distributed in California, Illinois, and New Jersey.
Sedecal recalled two units of its Mobile X-ray system on June 10, 2025. Users must stop using the device due to improper cleaning risks. The equipment is not water-resistant, posing a high hazard to patients and healthcare providers.
SEDECAL SA recalled five units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant, posing a risk if not cleaned properly. Users must follow strict cleaning guidelines to avoid serious consequences.
SEDECAL SA recalled 268 units of the Model Number 40KWFXPLUS Mobile X-ray system on June 10, 2025. The recall addresses concerns over improper cleaning and water resistance. Healthcare providers must stop using the device immediately and follow the manufacturer’s instructions.
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.