International safety notice
Corrective action for Advia 1800 und Advia 2400 ISE Firmware V2.23, Siemens
Germany / BfArM · DEU · Feb 14, 2014
Key facts
| Title | Corrective action for Advia 1800 und Advia 2400 ISE Firmware V2.23, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Advia 1800 und Advia 2400 ISE Firmware V2.23, Siemens |
| Manufacturer | Corrective action for Advia 1800 und Advia 2400 ISE Firmware V2.23, Siemens |
| Models | 10591, V2.23, 14-01, V2.22, 10817232 |
| Date | Feb 14, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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