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

Recall Z-1278-2013 — DePuy Mitek Tissue Liberator -Blade Up Catalog Number: 214623 The Reusable Arthroscopy Instruments are reusable, non-powered surgical instruments used during arthroscopic surgery of any joint except the spine.

U.S. FDA — Device Enforcement · United States · 2013-04-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1278-2013
Date of alert
2013-04-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
DePuy Mitek, Inc., a Johnson & Johnson Co.
Product category
device
Product type
Devices
Reported risk: Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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