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Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915
Recalled August 28, 2019 · FDA recall Z-2343-2019 · Siemens Medical Solutions USA
Hazard
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly. · FDA Class II
Units
44
Sold at
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Description
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Product
MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →