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

Recall Z-0695-2020 — Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C

U.S. FDA — Device Enforcement · United States · 2019-11-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0695-2020
Date of alert
2019-11-14
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)
10094142
Reported risk: In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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