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

Recall Z-1770-2017 — Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems

U.S. FDA — Device Enforcement · United States · 2016-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1770-2017
Date of alert
2016-10-17
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)
10684336
Reported risk: Due to a potential manufacturing error, a rare possibility exists for a sudden drop in table height of the Combi Dockable Table Neurosurgery.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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