International safety notice
Recall for the blood products CompoStop and Compoflex, Fresenius Kabi
Germany / BfArM · DEU · Feb 10, 2014
Key facts
| Title | Recall for the blood products CompoStop and Compoflex, Fresenius Kabi |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the blood products CompoStop and Compoflex, Fresenius Kabi |
| Manufacturer | Recall for the blood products CompoStop and Compoflex, Fresenius Kabi |
| Models | T5000, 40G105GAOO, 40GH30GAOO, T4001, 40G110ABOO, 40GH30ABOO, 40GH29GAOO, 40GH23GBOO, 06172-686-5080, T3961, 812738852, 40G103AAOO and 15 more |
| Date | Feb 10, 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