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

Recall Z-2271-2015 — Fabius MRI Anesthesia Machine; Fabius MRI is an inhalation anesthesia machine for use in MRI environments in operating, induction and recovery rooms.

U.S. FDA — Device Enforcement · United States · 2015-06-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2271-2015
Date of alert
2015-06-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Draeger Medical, Inc.
Product category
device
Product type
Devices
Reported risk: the Fabius MRI or parts of the system were attracted by the magnetic field of the MRI. If the Fabius MRI is positioned too close to the MRI, its parts can be loosened as a result of the magnetic force of the MRI.
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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