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

Recall Z-0696-2020 — smith&nephew PROFIX Mallet, 750 GRAMS, REF 71512452 - Product Usage: The PROFIX Mallet is a reusable surgical instrument used to tap instruments or implants during knee or hip surgery.

U.S. FDA — Device Enforcement · United States · 2019-11-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0696-2020
Date of alert
2019-11-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
71512452
Reported risk: There is a a potential failure mode associated with the use of the mallet, wherein the poly tip of the mallet may become loose and/or come off during use. If the potential failure mode occurs, particles generated in the poly thread potentially could enter the surgical field or a delay in surgery could occur if the tip disengages during the use of the mallet.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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