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

Recall Z-0964-2013 — Howmedica Osteonics Corp. Stryker Orthopaedics Specialty Triathlon Left and Right A//P Sizer Adjustment Housing PER File K2401. For use in knee prosthesis implantation. NON-STERILE

U.S. FDA — Device Enforcement · United States · 2013-01-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0964-2013
Date of alert
2013-01-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Howmedica Osteonics Corp.
Product category
device
Product type
Devices
Reported risk: The standard Triathlon Femoral Stylus does not fit into the Specialty Sizers and the "R" and "L" markings on the Right Sizer are reversed.
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.

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