1,046 recalls tagged with “electrical hazard”.
FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.
UIH Technologies LLC is recalling 4 Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT systems sold in the United States. A third-party outer cover can become trapped between the patient table and gantry during table movement. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions.
GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM
GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.
GE HealthCare Israel recalled 37 Maxicam dual-head gamma cameras distributed worldwide to hospitals. The recall cites potential detector mounting stress if the devices are moved without adequate support. This could result in a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the device and follow recall instructions from GE HealthCare.
GE HealthCare is recalling 28 Elscint SPX6 dual-head gamma cameras worldwide. The recall cites detectors could be stressed during transport or relocation without adequate detector support, risking a detector fall and life-threatening injury. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.
Philips North America recalls 28 Cardiac Workstation 5000 devices, model 860439, distributed nationwide in five states. A pinched power module wire led to a short during environmental stress tests. Users should stop using the device and follow manufacturer recall instructions.
UIH Technologies recalls 3 units of Shanghai United Imaging Healthcare uMI 780 PET/CT systems after a third-party outer cover can trap between the patient table and gantry. The issue can obstruct table movement. Hospitals are urged to stop using the devices and follow recall instructions.
Mars Foods US recalled 1,075 cases of Ben's Original Ready Rice Long Grain & Wild 8.8 oz sold in nine states. The hazard is the possible presence of stones in the product. Consumers should not consume the product and should contact Mars Foods US for refund or replacement by email.
GE HealthCare recalled 292 Millenium MPR dual-head gamma cameras worldwide after discovering some units past End of Guaranteed Service may have been transported without adequate detector support. This can place excessive stress on detector mounting and could result in a detector fall with life-threatening injury. Healthcare facilities should stop using the devices immediately and follow recall PIN
GE HealthCare recalled 1 Optima NX dual-head gamma camera worldwide after detecting potential detector mounting failure if the unit is moved without proper support. The risk could cause a detector fall and life-threatening injury. Hospitals should stop using the device and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging for guidance.
In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.
Epoca International recalls Paris Hilton mini beauty fridges sold before August 2024 due to a shorting electrical switch that can overheat and cause a fire. Consumers should stop using the recalled units and seek a full refund. Details and how to claim are on Epoca’s recall page or by phone.
Olympus Corporation of the Americas recalls 8,587 bronchovideoscope units worldwide, including 4,297 in the US and 4,290 outside. The recall centers on updated IFU language for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Stop using the device immediately and follow manufacturer instructions for remediation.
Olympus Corporation of the Americas recalls its BF-P150 bronchoscope after updates to the instruction for use. The recall covers 1,019 units outside the U.S. Distribution was nationwide in the U.S. The agency classifies this as a high-hazard issue.
Olympus Corporation of the Americas recalls 361 units in the US and 258 units overseas as of September 11, 2025. The recall targets the EVIS EXERA b Bronchovideoscope BF-XT190. The update adds safety instructions for using bronchoscopes with laser, argon plasma coagulation, and high-frequency therapy equipment. Patients and healthcare providers should stop using the device immediately and follow a
Boston Scientific recalled 172 units of the CXR Preconnect with TENACIO Pump with InhibiZone worldwide. The recall was initiated on 2025-09-11 and remains active as of 2025-10-22. The devices can experience inflation and/or deflation performance issues. Healthcare providers should stop using the devices and follow manufacturer instructions for recall remediation.
Olympus Corporation of the Americas reports an active recall for the BRONCHOVIDEOSCOPE BF-1TH1100. The recall concerns additional IFU updates for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. The company urges stopping use and following recall instructions.
Boston Scientific is recalling 1 CX Preconnect with TENACIO Pump sold to healthcare providers worldwide, including the US and Canada. The device may experience inflation and/or deflation performance issues. Healthcare providers and patients should stop using the device and follow manufacturer recall instructions.
CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from