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

Recall Z-3262-2018 — HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide va

U.S. FDA — Device Enforcement · United Kingdom · 2018-08-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3262-2018
Date of alert: 2018-08-09
Country / jurisdiction: United Kingdom
Risk level: Class II
Risk type: recall
Brand: Biomet UK Ltd.
Product category: device
Product type: Devices

Reported risk: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel

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.

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