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Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Pate
Recalled July 9, 2014 · FDA recall Z-1978-2014 · Stryker Howmedica Osteonics
Hazard
Tritanium Patella Inserter Instrument fracture during implantation. . · FDA Class II
Units
22 Units
Sold at
US Nationwide Distribution - in the states of Arizona, Florida, Kentucky, Louisiana and New Jersey.
Description
Tritanium Patella Inserter Instrument fracture during implantation. .
Product
Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the Tritanium Knee System Instrument Set. It is used to implant the Tritanium Patella after the patellar bone has been prepared using the existing Triathlon Patella Resection Guide, Metal Backed Patella Drill and Patella Peg Drill Templates as per the Triathlon Tritanium Surgical Protocol.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →