International safety notice
Recall for Omniflush, B. Braun Melsungen AG
Germany / BfArM · DEU · Apr 8, 2011
Key facts
| Title | Recall for Omniflush, B. Braun Melsungen AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Omniflush, B. Braun Melsungen AG |
| Manufacturer | Recall for Omniflush, B. Braun Melsungen AG |
| Models | S10349, S10344, 3570260, 42690900, S10342, 34212, S10337, S10126, S10192, 3570230, S10274, S10271 and 9 more |
| Date | Apr 8, 2011 |
| 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