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

Recall Z-1310-2021 — Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.

U.S. FDA — Device Enforcement · United States · 2021-02-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1310-2021
Date of alert
2021-02-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Arthrex, Inc.
Product category
device
Product type
Devices
Reported risk: The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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