Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Evergreen Orchard Farm recalled 610 cases of Korean Pear Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The affected product was distributed to Pennsylvania, New Jersey, and New York. Consumers should not consume this juice and are advised to seek refunds or replacements.
Tandem Diabetes Care recalled 19 t:slim X2 Insulin Pumps on July 3, 2025, due to an app defect. The defect affects devices when set to right-to-left languages, potentially causing incorrect therapy decisions. This may lead to hypoglycemia or hyperglycemia.
Evergreen Orchard Farm recalled 78 cases of grape juice on July 3, 2025, due to a lack of pasteurization and sanitation records. The recall affects products distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds.
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.
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 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 22 units of its Model SM-32HF-Batt Mobile X-ray system on June 10, 2025. The recall alerts users that the equipment is not water-resistant and requires strict cleaning per the manual. Improper cleaning may lead to serious safety risks.
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 SA recalled its Mobile X-ray system on June 10, 2025, due to a water resistance hazard. The company alerted users to strictly follow cleaning instructions to avoid potential harm. The recall affects devices distributed in California, Illinois, and New Jersey.
Sedecal recalled 12 units of its Mobile X-ray system on June 10, 2025. The equipment lacks water resistance and poses a high hazard if not cleaned properly. Users must follow strict cleaning protocols to avoid serious consequences.
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 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.