International safety notice
Recall of PO830SU / PO831SU / PO833SU, Aesculap AG
Germany / BfArM · DEU · Feb 18, 2016
Key facts
| Title | Recall of PO830SU / PO831SU / PO833SU, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of PO830SU / PO831SU / PO833SU, Aesculap AG |
| Manufacturer | Recall of PO830SU / PO831SU / PO833SU, Aesculap AG |
| Date | Feb 18, 2016 |
| 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