Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0744-2017 — SOMATOM Definition Edge System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles

U.S. FDA — Device Enforcement · United States · 2016-11-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0744-2017
Date of alert
2016-11-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10590000
Reported risk: Software update that provides software and firmware bug-fixes to improve system performance
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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