FDA recall record

Toshiba American Medical Systems INFX-8000V Fluoroscopic X-Ray Systems recall — FDA Z-0844-2018

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…

Class IIclassification
Z-0844-2018official record ID
Mar 14, 2018report date

Recall record at a glance

Official recordZ-0844-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmToshiba American Medical Systems Inc.
Report dateMar 14, 2018
Recall initiation dateDec 29, 2017
Quantity29 units
LocationTustin, CA, United States

Official product description

INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM

Why the product 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.

Distribution information

United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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