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

Recall Z-1202-2014 — Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray

U.S. FDA — Device Enforcement · United States · 2013-12-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1202-2014
Date of alert
2013-12-05
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)
10848280
Reported risk: There exists the possibility that during clinical operation, a breakdown of the x-ray tube could result in loss of x-ray imaging for the Artis Q and Artis Q biplane systems with a flat detector as 40 HDR (large 30x40).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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