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

Recall Z-2244-2012 — Medtronic O-arm¿ Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R.

U.S. FDA — Device Enforcement · United States · 2012-07-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2244-2012
Date of alert
2012-07-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Navigation, Inc.
Product category
device
Product type
Devices
Reported risk: A fault in a high voltage relay in the 0-arm¿ Imaging System might cause the relay to overheat and burn.
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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