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

Recall Z-1684-2016 — Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone screw 6.5x15 selftap 00625006515 Bone screw 6.5x20 selftap 00625006520 Bone screw 6.5x25 selftap 00625006525 Bone screw 6.5x30 selftap 00625006530

U.S. FDA — Device Enforcement · United States · 2016-05-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1684-2016
Date of alert
2016-05-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Manufacturing B.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
63284570
Reported risk: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
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.

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.