International safety notice
Recall of Surgical Instrumentkit for THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis
Germany / BfArM · DEU · Jul 14, 2006
Key facts
| Title | Recall of Surgical Instrumentkit for THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis |
| Manufacturer | Recall of Surgical Instrumentkit for THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis |
| Models | 421EEC, CE-1NRHNG, IS00111S005, IS005, 42FEEC |
| Date | Jul 14, 2006 |
| 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