International safety notice
Corrective action for Immulite 2000 / 2500 Androstenedione, Siemens
Germany / BfArM · DEU · Sep 11, 2009
Key facts
| Title | Corrective action for Immulite 2000 / 2500 Androstenedione, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Immulite 2000 / 2500 Androstenedione, Siemens |
| Manufacturer | Corrective action for Immulite 2000 / 2500 Androstenedione, Siemens |
| Models | GPF-003-6, 07836, L2KAO, 973.927.2828, 2009-01-19, L5KAO |
| Date | Sep 11, 2009 |
| 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