International safety notice
Corrective action of Bayer for Advia 1200, Advia 1650 and Advia 2400 Systems
Germany / BfArM · DEU · Mar 24, 2006
Key facts
| Title | Corrective action of Bayer for Advia 1200, Advia 1650 and Advia 2400 Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Advia 1200, Advia 1650 and Advia 2400 Systems |
| Manufacturer | Corrective action of Bayer for Advia 1200, Advia 1650 and Advia 2400 Systems |
| Models | 125.0, 10591-5097, 073D0182-01, 2006-02, 135.0 |
| Date | Mar 24, 2006 |
| 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