These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,168 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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.
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 its Mobile X-ray system, model 40KWFXPLUS.889, on June 10, 2025. The device is not water-resistant and improper cleaning can lead to serious issues. One unit distributed in California, Illinois, and New Jersey is affected.
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 five units of its Mobile X-ray system on June 10, 2025. The equipment poses a high hazard due to its lack of water resistance and improper cleaning risks. Users must stop using the device immediately and follow the recall instructions.
Sedecal recalled one unit of its Mobile X-ray system on June 10, 2025. The equipment lacks water resistance and requires strict cleaning protocols. Users should stop using the device immediately to avoid potential hazards.
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.