International safety notice
Advisory Notice from Smith & Nephew for Macrotetured Profix and Genesis II femoral components
Germany / BfArM · DEU · Mar 31, 2005
Key facts
| Title | Advisory Notice from Smith & Nephew for Macrotetured Profix and Genesis II femoral components |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Macrotetured Profix and Genesis II femoral components |
| Manufacturer | Advisory Notice from Smith & Nephew for Macrotetured Profix and Genesis II femoral components |
| Models | 9514950, 9514-148, 22869, 14-275, 839003-34, 34253, 683-9234, 001-901 |
| Date | Mar 31, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching catalog numbers in FDA data
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