International safety notice
Corrective action for the Prismaflex® control unit used together with the PrismaLung™ Kit, Gambro
Germany / BfArM · DEU · Nov 3, 2014
Key facts
| Title | Corrective action for the Prismaflex® control unit used together with the PrismaLung™ Kit, Gambro |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Prismaflex® control unit used together with the PrismaLung™ Kit, Gambro |
| Manufacturer | Corrective action for the Prismaflex® control unit used together with the PrismaLung™ Kit, Gambro |
| Models | 003-2014, FA-2014-007 |
| Date | Nov 3, 2014 |
| 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