International safety notice
Recall of Compoflex® and Composelect® bloodbag systems, Fresenius Kabi
Germany / BfArM · DEU · Aug 24, 2015
Key facts
| Title | Recall of Compoflex® and Composelect® bloodbag systems, Fresenius Kabi |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Compoflex® and Composelect® bloodbag systems, Fresenius Kabi |
| Manufacturer | Recall of Compoflex® and Composelect® bloodbag systems, Fresenius Kabi |
| Models | XX-JUN-2015, PQ31150, PQ32250, PQ32150, 41IB06AA00, 41IB03AA00, 41IA25FA00, 41IB01AA00 |
| Date | Aug 24, 2015 |
| 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