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Toshiba American Medical Systems Inc recalls INFX-8000F Fluoroscopic X-Ray Systems
Recalled March 14, 2018 · FDA recall Z-0842-2018 · Toshiba American Medical Systems
Hazard
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. · FDA Class II
Units
17 units
Sold at
United States
Description
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.
Product
INFX-8000F Fluoroscopic X-Ray Systems
Manufacturer(s)
Toshiba American Medical Systems Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →