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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:112591

"***PressFT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture***NP261***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures

Official recall number

Z-0064-2013

Evidence summary

Product code
MBI
Recall status
Terminated
Event initiated
June 26, 2012
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0064-2013