Siemens Medical Solutions USA, Inc recalls SOMATOM go.Top; Models #11061648 Product Usage: This computed tomography system is intended to generate and process cro…
- Recall date
- July 31, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2405-2019
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- US Nationwide Distribution in the states FL KS WI NE MS OH TX NY LA IN IL OK MI GA NJ AK CT AL MD
Why it was recalled
The injector holder could potentially fall off together with the injector and the storage box.
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 go.Top; Models #11061648 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
Get recall alerts
Free email alert whenever Siemens Medical Solutions USA, Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Siemens Medical Solutions USA, Inc