1,814 product recalls found in this category. Browse through all safety alerts and stay informed.
High Activity Category
This category has a significant number of recalls. Please check regularly for updates.
Sedecal SA recalls a single SM-20HF-Batt 20KW analog mobile X-ray system distributed in the United States and Canada after notifying consignees via email. The device is not water-resistant and must be cleaned strictly as described in the manual. Improper cleaning could cause safety or equipment issues.
Sedecal SA recalled 4 SM-40HF-B-D-C 40KW mobile X-ray systems sold in California, Illinois and New Jersey. A notice warns the equipment is not water-resistant and must be cleaned exactly as described in the manual to avoid possible consequences of improper cleaning. Healthcare providers should stop using the device immediately and contact Sedecal SA or their provider for 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 6 mobile X-ray systems in the United States on June 10, 2025 after warning that the devices are not water-resistant and must be cleaned strictly per the manual. The recall notes possible consequences of improper cleaning. Healthcare facilities should stop using the devices 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 recalled 1 Mobile X-ray system due to major safety concerns. The device is not water-resistant and improper cleaning can cause malfunctions. Healthcare providers and patients must stop using the system immediately and follow manufacturer 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 recalled 2 units of the SM-40HF-B-D-C 40KW 55G/60G Mobile X-ray system after warning consignees that the device is not water-resistant and must be cleaned exactly according to the manual. The notice outlines the potential consequences of improper cleaning. Healthcare facilities in California, Illinois and New Jersey should stop using the device immediately and contact Sedecal for further 1
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 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 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 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 mobile X-ray systems in the United States, including units distributed to California, Illinois and New Jersey. The devices are not water-resistant and must be cleaned strictly per the manual to avoid safety risks. Stop using the device immediately and follow the manufacturer’s recall instructions.
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.
Medtronic MiniMed recalled 1,440 Simplera Sensor units distributed outside the United States after a device cap label may not adhere, risking sterility. The defect could increase infection risk. Patients and healthcare providers should stop using the device and follow recall instructions provided by Medtronic MiniMed or their healthcare provider.
3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets due to incorrect flow rates and outlet temperature locations. This defect can affect the warming of fluids, posing serious risks to patients. Healthcare providers must stop using these devices immediately and follow the manufacturer’s instructions for returns.
World Perfumes Inc. recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic in Florida after broken or leaking containers were reported. The recall covers iodine 2% antiseptic distributed by Essential Products. Consumers should stop use immediately and contact World Perfumes or a healthcare provider for guidance.
MEDITECH released an active recall for the Expanse Laboratory calculator/data processing module. The recall covers 148 units distributed worldwide, including the US, UK, Canada, Ireland and the British Virgin Islands. The hazard concerns simultaneous multi-key inputs potentially removing data from the first field in screens or questionnaires.
CorNeat Vision recalled EverPatch surgical matrix (REF 1036295) in a worldwide distribution that includes 50 states and several countries. The recall addresses retroactive labeling corrections to include prevention and management of would dehiscence. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.