International safety notice
Corrective Action for IMMULITE 2000/2000 XPi Erythropoietin and IMMULITE 2500 Erythropoietin, Siemens
Germany / BfArM · DEU · May 30, 2012
Key facts
| Title | Corrective Action for IMMULITE 2000/2000 XPi Erythropoietin and IMMULITE 2500 Erythropoietin, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE 2000/2000 XPi Erythropoietin and IMMULITE 2500 Erythropoietin, Siemens |
| Manufacturer | Corrective Action for IMMULITE 2000/2000 XPi Erythropoietin and IMMULITE 2500 Erythropoietin, Siemens |
| Models | 10591, L2KEPN2, L5KEPN2 |
| Date | May 30, 2012 |
| 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