FDAFDA · Food and drugs·Recall number Z-2130-2013
Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No. 6541-2-609), for use in Total Knee Arthroplasty (TKA) when the surgeon elects to use Stryker's Triathlon Total Knee System in conjunction with EM referencing. Non-Sterile Instrument.
Published September 4, 2013 · Recall initiated: July 2, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Howmedica Osteonics Corp.
- Distributor
- Nationwide Distribution
- Lot
- Catalog #6541-2-609 All lot codes
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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