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

Recall Z-1586-2014 — INSTRUMENT TRACKER 9733533XOM ENT 1PK

U.S. FDA — Device Enforcement · United States · 2014-04-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1586-2014
Date of alert
2014-04-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Navigation, Inc.
Product category
device
Product type
Devices
Reported risk: Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.
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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