International safety notice
Batch recall for Endobon Xenograft Granules, Biomet France SARL / BIOMET 3i Deutschland GmbH
Germany / BfArM · DEU · Mar 22, 2016
Key facts
| Title | Batch recall for Endobon Xenograft Granules, Biomet France SARL / BIOMET 3i Deutschland GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Endobon Xenograft Granules, Biomet France SARL / BIOMET 3i Deutschland GmbH |
| Manufacturer | Batch recall for Endobon Xenograft Granules, Biomet France SARL / BIOMET 3i Deutschland GmbH |
| Models | V0021168, T0035073, T0281078, U0092189, U0044155, U0261187, T0064164, T0292065, T0183280, V0134208, U0114307, U0035237 and 275 more |
| Date | Mar 22, 2016 |
| 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