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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:135950

Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint

Official recall number

Z-1635-2015

Evidence summary

Product code
JWH
Recall status
Terminated
Event initiated
August 15, 2014
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1635-2015

Field note

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