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

Recall Z-1602-2016 — Medtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use in neurosurgery.

U.S. FDA — Device Enforcement · United States · 2016-04-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1602-2016
Date of alert
2016-04-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Sofamor Danek Usa, Inc - Dallas Distribution
Product category
device
Product type
Devices
Reported risk: Incorrect color coding and attachment reference were included on the labeling of 10BA40D dissecting tools with lot number H5237248.
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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