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Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp. Recalls

All product recalls associated with Stryker Howmedica Osteonics Corp..

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Recall Summary

Total Recalls

252

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 121–140 of 252 recalls

Stryker Howmedica Osteonics Corp.: Triathlon Revision Instruments; 1,2,7,8 TGC Upper Tray; N...

Laceration Risk

The screen print for the Valgus Adapter catalog numbers on the Triathlon Trial Cutting Guide Instrument Trays is incorrect.

FDAMay 15, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 4MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

FDAApr 16, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 2MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

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FDAApr 16, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 6MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

FDAApr 16, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 8MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

FDAApr 16, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Restoration Modular Cone Bodies; titanium Alloy and Hydro...

Packaging burst test values for the Restoration Modular Cone Body family were found to be incorrectly transferred from the finalized validation to the work specification. Testing showed that burst test results for recalled products fell below the validated parameters.

FDAApr 2, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker, Gamma3 Plus Obese Targeting System, Operative Te...

Operative Technique: further clarification and guidance is needed to help reduce the potential for distal mis-drilling of the short Gamma3 Trochanteric Nails.

FDAMar 2, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker, Gamma3S Trochanteric Nail 170, Operative Techniq...

Operative Technique: further clarification and guidance is needed to help reduce the potential for distal mis-drilling of the short Gamma3 Trochanteric Nails.

FDAMar 2, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker, Gamma3, The Compact Version of the Gamma Nail Sy...

Operative Technique: further clarification and guidance is needed to help reduce the potential for distal mis-drilling of the short Gamma3 Trochanteric Nails.

FDAMar 2, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Modular Replacement System (MRS) Cemented Stems, Sterile,...

Instruction for use incorrect: There are no statements or warning on labels or Instructions for Use that 8, 9 and 10 mm diameter MRS Cemented Stems are indicated only for use in the GMRS Proximal Tibial and Distal Femoral Components.

FDAJan 30, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker Howmedica Osteonics, Primary Super SecurFit Stem...

Stryker Orthopaedics became aware that there may be difficulty in mating stem to implantation/extraction instrument.

FDAJan 14, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker Howmedica Osteonics, Super SecurFit HA Hip Stem;...

Stryker Orthopaedics became aware that there may be difficulty in mating stem to implantation/extraction instrument.

FDAJan 14, 2009Nationwide• Stryker Howmedica Osteonics Corp.