International safety notice
Fresenius Kabi: Safety Notice for the blood bag systems COMPOFLOW, COMPOSTOP, COMPOFLEX and COMPOSELECT
Germany / BfArM · DEU · Mar 24, 2014
Key facts
| Title | Fresenius Kabi: Safety Notice for the blood bag systems COMPOFLOW, COMPOSTOP, COMPOFLEX and COMPOSELECT |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the blood bag systems COMPOFLOW, COMPOSTOP, COMPOFLEX and COMPOSELECT |
| Manufacturer | Fresenius Kabi: Safety Notice for the blood bag systems COMPOFLOW, COMPOSTOP, COMPOFLEX and COMPOSELECT |
| Models | 43GL15FA00, 43GL15FB00, PD51600, 40HB05AC00, 41HA20FA00, C5000, 41GL29GA00, 41HA10FA00, 43GL01FA00, 40HA29FA00, 43GL19FA00, 41HA06FA00 and 46 more |
| Date | Mar 24, 2014 |
| 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