Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:143882

Product 57 consists of all product code: JDI and same usage: Item no: 763401000 PRESSFIT FEM ST FX 10 X 115 763401100 PRESSFIT FEM ST FX 11 X 1 763401200 PRESSFIT FEM ST FX 12 X 1 763401300 PRESSFIT FEM ST FX 13 X 1 763401400 PRESSFIT FEM ST FX 14 X 1 763401500 PRESSFIT FEM ST FX 15 X 1 For use in total or hemi hip arthroplasty

Official recall number

Z-1155-2016

Evidence summary

Product code
JDI
Recall status
Terminated
Event initiated
January 11, 2016
Root cause
Packaging
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1155-2016

Field note

Send feedback

We'll only use this to respond to your feedback.