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

Recall Z-1264-2018 — IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600

U.S. FDA — Device Enforcement · United States · 2018-02-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1264-2018
Date of alert
2018-02-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Deerfield Imaging, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10006997
Reported risk: The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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