International safety notice
Corrective action and recall of DPC Biermann for Immulite 2000 and Immulite 2500 systems
Germany / BfArM · DEU · Mar 7, 2006
Key facts
| Title | Corrective action and recall of DPC Biermann for Immulite 2000 and Immulite 2500 systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Immulite 2000 and Immulite 2500 systems |
| Manufacturer | Corrective action and recall of DPC Biermann for Immulite 2000 and Immulite 2500 systems |
| Models | 811498576, 21.03.2005, 2444S, 9262-222, 9262-0, 16593, 10-1000, 43028, 5-50P11, 9262-111, D-68723, 06202 |
| Date | Mar 7, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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