International safety notice
Recall for the Plasmafit Biolox delta Insert Type G head diameter 36 mm, Aesculap AG
Germany / BfArM · DEU · Jan 15, 2015
Key facts
| Title | Recall for the Plasmafit Biolox delta Insert Type G head diameter 36 mm, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Plasmafit Biolox delta Insert Type G head diameter 36 mm, Aesculap AG |
| Manufacturer | Recall for the Plasmafit Biolox delta Insert Type G head diameter 36 mm, Aesculap AG |
| Models | NH102D, 14-12-22, 78501, NV213, 52080304, 78532, 52074933, 2014-12-22, 6119B_, 1262TN, DEULDESS653 |
| Date | Jan 15, 2015 |
| 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