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

Recall Z-0663-2018 — NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral condyle of the knee joint in Total Knee Arthroplasty.

U.S. FDA — Device Enforcement · Ireland · 2017-07-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0663-2018
Date of alert
2017-07-24
Country / jurisdiction
Ireland
Risk level
Class II
Risk type
recall
Brand
ZIMMER ORTHOPEDIC MFG LTD
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
63329529
Reported risk: There is a possibility that the protective foam insert used during the packaging of the affected products is undersized, which may cause a breach in the inner cavity during transportation.
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.