International safety notice
Recall for the DA360 Knee system, Biomet
Germany / BfArM · DEU · Jan 3, 2012
Key facts
| Title | Recall for the DA360 Knee system, Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the DA360 Knee system, Biomet |
| Manufacturer | Recall for the DA360 Knee system, Biomet |
| Models | ‘DA360’, 607646, DA360’, DA360, SSK360, 512235 |
| Date | Jan 3, 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