Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Quidel recalls 22,470 Rapid Strep A Dipstick tests sold worldwide, including multiple U.S. states. The dipstick test may yield false positive results. Health providers and patients should stop using the device immediately and follow recall instructions. Check with Quidel for refund or replacement options.
Vitalabs recalled 9,657 bottles of Vitamin B12 Raspberry Gummies sold under Black Girl Vitamins and Rise-N-Shine brands after suppliers flagged undeclared peanuts. The product may contain peanuts not disclosed on the label, creating a peanut allergy risk. Consumers should stop using the product and contact Vitalabs for refund or replacement.
Immunocore recalled 7,572 vials of KIMMTRAK (tebentafusp-tebn) Injection due to subpotency concerns. This defect may compromise treatment efficacy for patients. Healthcare providers and patients should stop using the product immediately and consult for guidance.
Sedecal SA recalls 10 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey. The recall stems from a warning that the equipment is not water-resistant and must be cleaned strictly according to the manual. Hospitals and providers should stop using the device immediately and contact Sedecal for instructions.
SEDECAL SA recalled 268 units of the 40KWFXPLUS Mobile X-ray System distributed in California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly according to the manual. Healthcare facilities should stop using the device immediately and await further recall instructions.
Sedecal SA recalls 1 unit of Model 40KWMOBILE3.899 Mobile X-ray system distributed to consignees in the United States, including California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly according to the manual, with the notice outlining the potential consequences of improper cleaning. Healthcare providers and patients should stop using the device immediat
Sedecal SA recalled 6 units of the SM-40HF-B-D-C 40KW Canon Ready Mobile X-ray System sold in California, Illinois and New Jersey. The company warned the equipment is not water-resistant and must be cleaned strictly per the manual to avoid possible consequences of improper cleaning. Users should stop using the device immediately and follow recall instructions provided by the manufacturer.
Sedecal SA recalled 12 units of the 40KWFXPLUS-710CW Mobile X-ray system distributed to CA, IL and NJ. The recall cites that the equipment is not water-resistant and must be cleaned strictly per the manual to avoid consequences of improper cleaning. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.
Sedecal SA recalled 22 SM-32HF-Batt 32KW analog mobile X-ray systems distributed to California, Illinois and New Jersey. The units are not water-resistant and must be cleaned strictly per the manual, with explicit consequences for improper cleaning. Healthcare facilities should stop using the devices immediately and follow the manufacturer's recall instructions sent by email.
Sedecal SA recalled 1 unit of the 40KW-FX.899 Mobile X-ray System distributed to CA, IL and NJ. The device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause adverse effects. Stop using the device and contact Sedecal SA or a healthcare provider for instructions.
SEDECAL SA recalled 1 unit of SM_40HF_BDC3 Mobile X-ray System distributed in California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly per the manual. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.
Sedecal recalled the Sed URS LP Mobile X-ray System in the United States, including CA, IL and NJ. The device is not water-resistant and must be cleaned strictly per the manual. Hospitals and healthcare providers should stop using the device immediately and follow Sedecal's recall instructions.
Sedecal SA recalls 6 units of the SM-40HF-B-D-C 40KW 80C Mobile X-ray system after warning consignees that the device is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could lead to safety risks. Hospitals and clinics in California, Illinois and New Jersey should stop using the device and follow the manufacturer's recall instructions.
Sedecal SA recalled 6 SM-40HF-B-D-C mobile X-ray systems distributed to consignees in California, Illinois and New Jersey after a notice reminded users the devices are not water-resistant and must be cleaned strictly per the manual. The reminder outlined possible consequences of improper cleaning. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.
Sedecal recalled 55 Mobile X-ray System units sold to facilities in California, Illinois and New Jersey. The devices are not water-resistant and must be cleaned exactly as described in the manual, with clear warnings about the consequences of improper cleaning. Hospitals and healthcare providers should stop using the device immediately and follow Sedecal's recall instructions.
Sedecal SA recalled 1 unit of the SM_40HF_BDC Mobile X-ray System distributed in California, Illinois and New Jersey after notifying consignees that the unit is not water-resistant and must be cleaned strictly per the manual. The notice cites potential consequences of improper cleaning. Hospitals and providers should stop using the device and follow the manufacturer’s recall instructions.
Sedecal SA is recalling the Shimadzu RF.004 Mobile X-ray System after warnings that the device is not water-resistant and must be cleaned strictly according to the manual. Hospitals in California, Illinois, and New Jersey are affected. Stop using the device and follow recall instructions.
Sedecal SA recalled 27 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after warning consignees the equipment is not water-resistant and must be cleaned per the manual. The notice outlines possible consequences of improper cleaning. Hospitals and providers should stop using the device immediately and follow recall instructions.
Sedecal SA recalls 24 RADPRO MOBILE mobile X-ray systems distributed in California, Illinois and New Jersey. A vendor notice warns the equipment is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have harmful consequences. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.
Sedecal SA recalled a single SM-40HF-B-D-C 40KW mobile X-ray unit distributed to California, Illinois and New Jersey. The device is not water-resistant and must be cleaned per the manual, with explicit warnings about improper cleaning. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.