International safety notice
Lot Recall of the product Endobon Xenograft Granules 0,5ml, Biomet 3i/ Biomet France
Germany / BfArM · DEU · Dec 11, 2013
Key facts
| Title | Lot Recall of the product Endobon Xenograft Granules 0,5ml, Biomet 3i/ Biomet France |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of the product Endobon Xenograft Granules 0,5ml, Biomet 3i/ Biomet France |
| Manufacturer | Lot Recall of the product Endobon Xenograft Granules 0,5ml, Biomet 3i/ Biomet France |
| Models | S0171081, S0171051, ROX05 |
| Date | Dec 11, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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