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

Recall Z-0061-2015 — Charnley PN Retract & Handle, REF 962004000, Non-Sterile-DuPuy International Ltd. The Charnley Pin Retractor and Handle Set is used to facilitate the insertion and extraction of two pins into and out of bone in the incision area, thereby holding the incision soft tissue open during the surgical p

U.S. FDA — Device Enforcement · United States · 2014-08-27 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0061-2015
Date of alert: 2014-08-27
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: DePuy Orthopaedics, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10603295240532

Reported risk: The small extraction peg of the Charnley Pin Retractor and Handle set is breaking from the pin.

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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