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

Recall Z-2619-2017 — DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

U.S. FDA — Device Enforcement · United States · 2017-05-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2619-2017
Date of alert
2017-05-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
DePuy Mitek, Inc., a Johnson & Johnson Co.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10886705026944
Reported risk: Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.