Toshiba American Medical Systems Inc recalls INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM
- Recall date
- December 29, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0844-2018
- FDA classification
- Class II
- Brand / firm
- Toshiba American Medical Systems Inc
- Sold / distributed
- United States
Why it was recalled
During an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the ceiling drive loosened cause the error.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM
Get recall alerts
Free email alert whenever Toshiba American Medical Systems Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Toshiba American Medical Systems Inc