International safety notice
Recall of UNI SCORE tibial tray / UNI SCORE femoral component / EXTREME diaphyseal nail / INITIALE modular femoral stem / INITIALE modular dysplastic femoral stem / INITIALE modular revision femoral stem / Extension stem for Total Knee Prosthesis / Allergy Solution extension stem for Total Knee Prosthesis, AMPLITUDE SAS
Germany / BfArM · DEU · Jun 20, 2016
Key facts
| Title | Recall of UNI SCORE tibial tray / UNI SCORE femoral component / EXTREME diaphyseal nail / INITIALE modular femoral stem / INITIALE modular dysplastic femoral stem / INITIALE modular revision femoral stem / Extension stem for Total Knee Prosthesis / Allergy Solution extension stem for Total Knee Prosthesis, AMPLITUDE SAS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Total Knee Prosthesis, AMPLITUDE SAS |
| Manufacturer | Recall of UNI SCORE tibial tray / UNI SCORE femoral component / EXTREME diaphyseal nail / INITIALE modular femoral stem / INITIALE modular dysplastic femoral stem / INITIALE modular revision femoral stem / Extension stem for Total Knee Prosthesis / Allergy Solution extension stem for Total Knee Prosthesis, AMPLITUDE SAS |
| Models | 1-0104314, 1-0205804, 1-0205802, 1-0160525, 1-02029XX, 1-0205801, 1-0202201, 1-0104354, 1-0104324, 1-02024XX, 1-0200741, 1-0200721 and 107 more |
| Date | Jun 20, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1