International safety notice
Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH
Germany / BfArM · DEU · Dec 17, 2012
Key facts
| Title | Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH |
| Manufacturer | Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH |
| Models | 65722, D-86916, 2.0.0, 4.2.2, 86916, 2.0.2, 2.0.3, 2012-12-20, 65722-0, 2012-11-30, 30-11-2012, 1.9.0 and 2 more |
| Date | Dec 17, 2012 |
| 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