1,120 recalls tagged with “electrical hazard”.
Makita U.S.A. recalls 3 cordless grease guns and 4 grease gun hoses due to a laceration hazard. Serial-numbered units are affected. Stop using the recalled equipment immediately and contact Makita for a free replacement hose.
StopBox USA recalls AR-15 Chamber Lock Pro shipped June 2 to July 15, 2025. The recall covers locks designed to chamber-lock AR-15 style rifles. The defect allows the lock to be forcibly removed, enabling unauthorized access to the firearm. StopBox urges immediate stop-use and provides refunds or replacements.
American Contract Systems recalled 32,433 radiology packs after a nonconformance during EO gas injection. The items were re-gassed and not validated for multiple sterilization cycles. The recall is active as of 2025-10-22. US distribution included SD, IA, MN, WA, IL. Health risks prompt immediate removal from use.
American Contract Systems recalled 32,433 medical convenience kits nationwide after finding re-gassed devices from EO sterilization. The recall affects five product lines with UDI-DI codes and Lot numbers. The re-gassing process has not been validated for multiple sterilization cycles, calling into question product safety and effectiveness. Health providers and patients should stop using these kit
American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide in SD, IA, MN, WA and IL. The devices were re-gassed after a nonconformance in the Ethylene Oxide sterilization process. The sterilization cycles have not been validated, so quality, safety and effectiveness cannot be confirmed. Consumers and healthcare providers should stop using the kits
American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process and have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using these products immediately and follow the manufacturer's recall.
American Contract Systems recalled 32,433 medical convenience kits nationwide in the United States after re-gassing sterilization cycles. The recall covers multiple packs including HEART PACK and PACEMAKER PACK with 2025 recall date. The safety issue centers on EO gasset validation failures after a nonconformance during initial gas injection. Stop using immediately and follow recall instructions.
Lutronic recalled 7,490 XERF EFFECTOR 60 electrosurgical units distributed worldwide, including several U.S. states, after manufacturing defects surfaced between April 1 and August 20, 2025. The defect can cause adverse events for patients. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalls 75 Allura Xper FD20/20 imaging systems due to potential deterioration of the CMOS battery, hard drive and power supply. Motorized movements could become unavailable while X-ray imaging remains functional. Operators should stop using affected units and follow manufacturer instructions.
Philips Medical Systems Nederland B.V. recalls 98 imaging systems worldwide after reports of component deterioration. Systems may lose motorized movements due to CMOS battery, hard disk drive, or power supply deterioration. Imaging remains available. Stop using the device and follow manufacturer instructions.
Philips Medical Systems Nederland B.V. recall involves 46 Allura CV20 imaging systems distributed worldwide. The devices may fail to perform due to deterioration of internal components including the CMOS battery, hard disk drive and power supply unit. If this occurs, motorized movements could become unavailable while imaging remains functional. The recall alerts patients and healthcare providers;停
Philips Medical Systems Nederland B.V. recalls 1 Allura Xper FD20/15 OR Table distributed worldwide to hospitals and clinics. The device may lose motorized movements due to deterioration of internal components. Stop using the device and contact Philips for instructions immediately.
Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.
Philips Medical Systems Nederland B.V. recalled 286 Allura Xper FD10/10 fluoroscopy systems worldwide, including 67 US units. Deterioration of internal components such as the CMOS battery, hard disk drive, and power supply can disable motorized system movements. Hospitals and other healthcare providers should stop using affected devices and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalls 2,114 Allura Xper FD20 imaging systems sold worldwide after reports that internal components may deteriorate. The recall covers models 722012, 722028 and 722006 with associated 510(k) numbers K102005 and K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949. If deterioration occurs, motorized movements may fail. Manual and imaging功能s,
The FDA confirms a nationwide recall of Zydus Lifesciences Chlorpromazine Hydrochloride tablets 200 mg (NDC 70710-1133-1) distributed by Zydus Pharmaceuticals USA. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable intake. Consumers and healthcare providers should stop using the product immediately and contact the distributor for guidance.
Philips Medical Systems Nederland B.V. recalled five Allura Xper FD20 Biplane OR Tables distributed worldwide after potential deterioration of the CMOS battery, hard disk drive and power supply could stop motorized movements. Hospitals and clinics should stop using the devices immediately and await manufacturer instructions.
Philips Medical Systems Nederland recalled 174 Allura Xper FD20 OR Tables worldwide, including 45 in the United States. The devices may deteriorate internally, rendering motorized movements inoperable. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions.
The FlexLab X System Potassium Test System was recalled by Inpeco S.A. on 2025-09-03 after the FDA identified an unvalidated hemolysis, icterus, and lipemia function in its Sample Integrity Module. The recall affects US distribution to California and New York. Stop using immediately and follow manufacturer instructions.