International safety notice
Lot Recall for Ostim 35, aap Biomaterials
Germany / BfArM · DEU · Mar 4, 2011
Key facts
| Title | Lot Recall for Ostim 35, aap Biomaterials |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ostim 35, aap Biomaterials |
| Manufacturer | Lot Recall for Ostim 35, aap Biomaterials |
| Models | 235110, 235102, 20.01.2010, 235105, 75019135, 235101, 12099, 228108, 35DELIVERY, 49-6071-929-100, 49-6071-929-0, 26.01.201 and 5 more |
| Date | Mar 4, 2011 |
| 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