International safety notice
Field Safety Corrective Action for HU35 / HCU20 / HCU30 / HCU40 systems, Maquet Cardiopulmonary GmbH
Germany / BfArM · DEU · Feb 17, 2016
Key facts
| Title | Field Safety Corrective Action for HU35 / HCU20 / HCU30 / HCU40 systems, Maquet Cardiopulmonary GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | HU35 / HCU20 / HCU30 / HCU40 systems, Maquet Cardiopulmonary GmbH |
| Manufacturer | Field Safety Corrective Action for HU35 / HCU20 / HCU30 / HCU40 systems, Maquet Cardiopulmonary GmbH |
| Models | HCU20I, 2015-12-10, 2015-11-30, HIJ35, HIJ35I, 2015-DEC, HCU20, 76437, FSCA-2015-12-10, FREIGEGE5EN, HCU40, HCU30I and 1 more |
| Date | Feb 17, 2016 |
| 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