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Ziehm Imaging Inc recalls Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
Recalled May 24, 2017 · FDA recall Z-1893-2017 · Ziehm Imaging
Hazard
During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component · FDA Class II
Units
US - 2 systems
Sold at
US Distribution to the states of : FL and CA. No devices listed in this recall where distributed any foreign /military/government consignees from the U.S.A.
Description
During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component
Product
Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
Manufacturer(s)
Ziehm Imaging Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →