International safety notice
Corrective action and recall of Dade Behring for the BEP 2000 and the BEP 2000 Advance System
Germany / BfArM · DEU · Dec 29, 2005
Key facts
| Title | Corrective action and recall of Dade Behring for the BEP 2000 and the BEP 2000 Advance System |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the BEP 2000 and the BEP 2000 Advance System |
| Manufacturer | Corrective action and recall of Dade Behring for the BEP 2000 and the BEP 2000 Advance System |
| Models | 39-3070, BR-29805.DOC, 496421-39-3070, 35001, 1.23.2, 496421-39 |
| Date | Dec 29, 2005 |
| 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