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

Recall Z-1605-2014 — Hinged Knee Support***LATEX FREE" Product Usage: Provide added lateral stability and allows the knee to tolerate more strenuous activity during recuperation.

U.S. FDA — Device Enforcement · United States · 2014-03-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1605-2014
Date of alert
2014-03-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Reported risk: During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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