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Stryker Howmedica Osteonics Corp. recalls Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No.
Recalled September 4, 2013 · FDA recall Z-2130-2013 · Stryker Howmedica Osteonics
Hazard
Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument. · FDA Class II
Units
10,537 units
Sold at
Nationwide Distribution
Description
Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Product
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.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →