International safety notice
Recall for the product Cannulated screw 7.5, aap Implantate AG
Germany / BfArM · DEU · Feb 24, 2015
Key facts
| Title | Recall for the product Cannulated screw 7.5, aap Implantate AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product Cannulated screw 7.5, aap Implantate AG |
| Manufacturer | Recall for the product Cannulated screw 7.5, aap Implantate AG |
| Models | 7532-80-2, 12099, 21044213 |
| Date | Feb 24, 2015 |
| 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