1,030 recalls tagged with “electrical hazard”.
Siemens Medical Solutions USA recalled 237 MAGNETOM Vida MRI scanners on August 28, 2025. The recall stems from a potential ice blockage in the magnet venting system which may cause helium leaks. The affected model number is 11060815, distributed worldwide, including the U.S.
Siemens Medical Solutions USA recalled 182 MRI machines on August 28, 2025, due to a risk of helium leaks. An ice blockage in the magnet venting system could cause pressure build-up, leading to a potential rupture. Users must stop using the device and follow recall instructions immediately.
Siemens Medical Solutions USA recalled 23 units of the Biograph mMR on August 28, 2025, due to a potential helium leak risk. The recall affects devices distributed worldwide, including the US. This Class I recall poses a high hazard to patients and healthcare providers.
Howmedica Osteonics recalled 55 units of surgical stems on August 28, 2025, due to a potential product mix. Packages labeled as Catalog Number 0580-1-442 may contain Catalog Number 0580-1-352, leading to possible patient safety risks.
Siemens Medical Solutions USA recalled one MRI scanner model due to a risk of helium leaks. The recall affects one unit distributed worldwide as of August 28, 2025. Users must stop using the device immediately and follow manufacturer instructions.
Siemens Medical Solutions USA recalled 39 MAGNETOM Prisma MRI scanners on August 28, 2025, due to a potential helium leak hazard. The recall affects units distributed worldwide, with a significant risk of helium gas build-up within the containment system. Healthcare providers must stop using the device immediately and follow recall instructions.
Siemens Medical Solutions USA recalled nine MRI scanners on August 28, 2025. The devices may develop ice blockages in the venting system, risking helium leaks. Healthcare providers must stop using the scanners immediately.
Siemens Medical Solutions USA recalled 69 units of the MAGNETOM Verio MRI system on August 28, 2025. Ice blockage in the magnet venting system could lead to a helium leak, posing serious risks. Healthcare providers must stop using the device immediately and follow recall instructions.
Siemens Medical Solutions USA recalled 27 units of its MAGNETOM Vida Fit MRI system on August 28, 2025. The recall addresses a risk of ice blockage that can cause helium gas pressure build-up. This defect may lead to a helium leak in the scanning room, posing a safety hazard.
Siemens Medical Solutions USA recalled the MAGNETOM Connectom.X. MRI Scanner on August 28, 2025. The recall affects one unit worldwide due to a potential helium leak risk. Users must stop using the device immediately as it poses a high hazard level.
Siemens Medical Solutions USA recalled 71 MRI machines on August 28, 2025. Ice blockages in the venting system may cause helium leaks. The recall affects models distributed worldwide, including the U.S.
Siemens Medical Solutions USA recalled 30 units of the MAGNETOM Skyra fit MRI system on August 28, 2025. The recall addresses a potential ice blockage in the magnet venting system that could lead to a helium leak. The device is distributed worldwide, including the US and multiple countries.
Vision RT recalled 56 AlignRT InBore systems on August 27, 2025, due to missing safety information in the Instructions for Use. The omission pertains to the identification and characteristics of the system's Class 1 lasers as required by federal regulations. Users must stop using the device immediately and follow manufacturer instructions.
W L Gore & Associates recalled over 52,000 vascular grafts on August 26, 2025, due to reports of delamination. The defect can lead to severe complications such as bleeding or cannulation difficulties. Affected products include multiple model numbers, which were distributed across the United States and internationally.
LeMaitre Vascular recalled 10 Artegraft Collagen Vascular Grafts on August 25, 2025, due to incorrect labeling. The devices lack CE and UKCA marks and are missing essential patient information. No distribution occurred within the U.S., but the affected products were sent to Great Britain and Switzerland.
GE Medical Systems recalled 29,225 units of the MAC VU360 Acquisition Trunk Cable and Module Holder on August 22, 2025. Users may incorrectly place the Acquisition Module, leading to cable damage and potential overheating. Affected devices were distributed globally, including the U.S. and several other countries.
Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance reflecting updated sample types and measurement ranges. Healthcare providers must stop using the device immediately and follow recall instructions.
Folsom Metal Products recalled 10 double packs of 14 mm Distraction Pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Healthcare providers and patients must stop using these devices immediately.
Folsom Metal Products recalled 10,960 units of 14 mm Distraction Pins on August 21, 2025. The recall follows concerns that the labeling included an unvalidated shelf life. Healthcare providers and patients must stop using the device immediately.
Folsom Metal Products recalled 2,700 units of distraction pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Patients and healthcare providers must stop using the product immediately.