2,679 recalls tagged with “immediate action”.
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 recalled 5 SM-40HF-B-D-C 40KW 55G Mobile X-ray systems distributed in the US (CA, IL, NJ) after warning that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice outlines the possible consequences of improper cleaning. Healthcare facilities should stop using the devices immediately and contact Sedecal SA for instructions.
Sedecal recalled 8 units of the Easy Moving Plus mobile X-ray system distributed in California, Illinois and New Jersey. The devices are not water-resistant and cleaning must follow the manual to avoid the consequences of improper cleaning. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.
Sedecal SA recalled 5 SM-40HF-B-D-C Mobile X-ray systems distributed in California, Illinois and New Jersey after notifying consignees via email. The notice says the equipment is not water-resistant and must be cleaned strictly per the manual. Hospitals and clinics should stop using the devices immediately and follow the recall instructions.
Sedecal SA recalled 8 mobile X-ray units in the United States after notifying consignees that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice warns that improper cleaning could have consequences described in the manual. Healthcare providers and patients should stop using the devices immediately and contact Sedecal SA or their healthcare provider for the
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 14 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after notifying consignees by email that the devices are not water-resistant. The company says cleaning must follow the manual strictly, warning about possible consequences of improper cleaning. Healthcare facilities and patients should stop using the devices immediately and follow the REMS
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 recalled 39 mobile X-ray systems due to a cleaning instruction issue that could cause improper maintenance. The recall affects units in the US and Canada. An email to consignees emphasizes the device is not water-resistant and must be cleaned per the manual, outlining potential consequences of improper cleaning. Healthcare facilities should stop using the device immediately and followSE
Sedecal SA recalled 1 mobile X-ray system in the United States. The device is distributed in CA, IL and NJ. The system is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have unspecified consequences. Clinicians and facilities should stop using the device and follow manufacturer 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.
Mercedes-Benz USA is recalling certain 2024 GLE 350 4MATIC, 2025 GLE 450e 4MATIC, and additional models sold through its dealer network. The issue involves a multi-purpose camera and rearview mirror that may detach from the windshield. Dealers will replace the windshield and reinstall the camera and mirror at no charge.
Mazda North American Operations recalls 2024-2025 Mazda3 and CX-30 vehicles after SAS units may deactivate airbags due to a low battery condition. Dealers will reprogram the SAS unit or replace it at no charge. Owner notification letters were mailed July 24, 2025.
Kia America recalls 2025 K5 sedans over a software error in the Power-net Domain Controller that can cause parking lights to flicker. The recall affects 2025 K5 vehicles. Dealers will update the PDC software, or owners can receive an OTA update for free. Letters notifying owners were mailed June 24, 2025. Contact Kia customer service at 1-800-333-4542. Recall SC341.
Steris recalled 10 units of the Barco MNA with HexaVue IP Integration System on May 23, 2025. A manufacturing error used an incorrect configuration file in a limited batch of adapter components. The recall is classified as Class II and affects states including Florida and Texas.
Volkswagen Group of America recalls 2024-2025 Atlas Cross Sport and Atlas vehicles for rearview camera distortion in reverse. The defect may reduce visibility behind the vehicle and increase crash risk. Dealers will update the camera control unit software free of charge. Owner letters mailed June 5, 2025. Contact VW customer service at 1-800-893-5298.
Chrysler recalls 2022-2025 Ram ProMaster vans for a rear-view camera issue. A software error in the security gateway module may prevent the rearview image from displaying. Dealers will update the software free of charge, and owner letters were mailed June 12, 2025.
PRIMO NO. 1 IN PRODUCE recalled 89 boxes of peeled-sliced cucumbers distributed to Virginia, New York, Pennsylvania and New Jersey after Salmonella contamination was detected. The recall was issued on May 20, 2025. Consumers should not eat the product and should contact PRIMO NO. 1 IN PRODUCE, INC for refund or replacement.
PRIMO NO. 1 IN PRODUCE recalls 89 boxes of Vegetable Tray Cucumbers distributed to Virginia, New York, Pennsylvania and New Jersey due to Salmonella contamination. Consumers should not consume the product. Contact PRIMO NO. 1 IN PRODUCE, INC for refund or replacement information via email, fax, letter, press release, telephone or visit.