International safety notice
Corrective action for the AV Sets with Recirculation System, B. Braun Avitum AG
Germany / BfArM · DEU · Apr 9, 2015
Key facts
| Title | Corrective action for the AV Sets with Recirculation System, B. Braun Avitum AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the AV Sets with Recirculation System, B. Braun Avitum AG |
| Manufacturer | Corrective action for the AV Sets with Recirculation System, B. Braun Avitum AG |
| Models | 7211161, 7211163, 03-05-07, DE210567578, 7211121, 2012-06, 95624383, 7211169, 7211122, AK100-200, 7211165, 20084008 and 11 more |
| Date | Apr 9, 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