International safety notice
Recall of orthopaedic implants from Biomet France
Germany / BfArM · DEU · Nov 23, 2006
Key facts
| Title | Recall of orthopaedic implants from Biomet France |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of orthopaedic implants from Biomet France |
| Manufacturer | Recall of orthopaedic implants from Biomet France |
| Models | 0000218682, 0000221758, 0000216112, 0000216087, 77-777-13450, SØÆ-DF0-Æ, 0000217184, ΡΟΙΟ4Ο2Β, 0000215280, 75-061000, 99C030.54, 900005 and 121 more |
| Date | Nov 23, 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