International safety notice
Recall of the connection component rotational version of the Endo-Model SL Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH
Germany / BfArM · DEU · Apr 16, 2012
Key facts
| Title | Recall of the connection component rotational version of the Endo-Model SL Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the connection component rotational version of the Endo-Model SL Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH |
| Manufacturer | Recall of the connection component rotational version of the Endo-Model SL Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH |
| Models | 16-0020, 16-2840, 02-2011, 02-2012 |
| Date | Apr 16, 2012 |
| 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