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

Recall Z-1840-2017 — Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: 72204039 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone

U.S. FDA — Device Enforcement · United States · 2017-03-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1840-2017
Date of alert
2017-03-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
72204039
Reported risk: Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
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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