Siemens Medical Solutions USA Recalls

26 recalls found for Siemens Medical Solutions USA. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)

Siemens Medical Solutions USA recalls MAGNETOM Spectra MRI with Model Number 10655588 after possible ice blockage in the magnet venting system could cause a helium leak during a quench. The recall covers worldwide distribution including the United States. Patients should stop using the device and follow manufacturer instructions for recall procedures.

Siemens Medical Solutions USA
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak

Siemens Medical recalled 27 MAGNETOM Vida Fit MRI systems after a potential helium containment rupture was identified. Ice blockage in the magnet venting system may prevent helium from escaping, leading to a dangerous pressure build-up. Patients and healthcare providers must stop using the device immediately and follow the manufacturer's instructions.

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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System

Siemens Medical Solutions USA issued a global recall for the MAGNETOM Connectom.X MRI system, Model 11371480. One unit is affected. A potential ice blockage in the magnet venting system could cause a helium leak during a quench. Users should stop using the device and await manufacturer instructions.

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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical Solutions USA MAGNETOM Prisma MRI Recalled for Ice Blockage Risk in 39 Units (2025)

Siemens Medical Solutions USA recalled 39 MAGNETOM Prisma MRI systems sold worldwide to healthcare providers. A potential ice blockage in the magnet venting system could prevent helium gas from escaping during a quench, causing pressure to build and potentially rupture the helium containment system. Hospitals and imaging centers using MAGNETOM Prisma should stop using the devices immediately and,,

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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Skyra fit MRI Recalled for Ice Blockage Risk in 30 Units (2025)

Siemens Medical Solutions USA recalled 30 MAGNETOM Skyra fit MRI units worldwide after identifying an ice blockage in the magnet venting system. The defect could prevent helium venting during a quench, causing pressure buildup that may rupture the helium containment and leak into the scanning room. Hospitals should stop using the affected devices immediately and follow the manufacturer’s recall,咨询

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Health & Personal Care
HIGH
FDA DEVICE

Siemens Artis Pheno Fluoroscopic X-Ray System Recalled for 20 Units in 2025

Siemens Medical Solutions USA is recalling 20 Artis Pheno image- intensifiied fluoroscopic X-ray systems distributed nationwide. The recall cites limited system movements after startup. Hospitals and healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

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Brand Statistics

Total Recalls
26
Pages
2

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