Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) Recalled by Stryker Howmedica Osteonics Corp. Due to Cracks or fracture of the Triathlon Tibial Alignment...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Howmedica Osteonics Corp. directly.
Affected Products
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.
Quantity: 10,537 units
Why Was This Recalled?
Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report