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

PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY — recall Z-1625-2015

U.S. FDA — Device Enforcement · United States · 2015-04-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1625-2015
Date of alert
2015-04-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wright Medical Technology, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
45304012
Reported risk: The term DORSAL was laser etched on the incorrect side on some of the angled handles.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.