Siemens Medical Solutions USA, Inc recalls SOMATOM Spirit(Model 10045692 )
- Recall date
- February 1, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2478-2018
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- Nationwide
Why it was recalled
A potential risk of unnecessary radiation exposure due to a software issue
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
SOMATOM Spirit(Model 10045692 )
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