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

Recall Z-2212-2012 — Trabecular Metal Reverse Shoulder Liner 40mm, part 00-4309-028-00 - Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Liner insertion by snapping the appropriate 60¿ (Standard) or 65¿ (Retentive) Poly Liner Impactor to the Poly Liner Impactor Handle. Then, place the Poly Liner Imp

U.S. FDA — Device Enforcement · United States · 2012-07-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2212-2012
Date of alert
2012-07-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
60443178
Reported risk: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are being recalled due to reports of alignment peg fractures. All lots of TM Reverse Shoulder Liner Impactors manufactured from 455 stainless steel are being retrieved, as all reported fractured instruments were manufactured with this material. The TM Reverse Shoulder Liner Impactor units that were manufactured with 13-8 stain
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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