International safety notice
Corrective Action for IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPI in combination with the IMMULITE IGF-I Control Module, Siemens
Germany / BfArM · DEU · Oct 26, 2012
Key facts
| Title | Corrective Action for IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPI in combination with the IMMULITE IGF-I Control Module, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPI in combination with the IMMULITE IGF-I Control Module, Siemens |
| Manufacturer | Corrective Action for IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPI in combination with the IMMULITE IGF-I Control Module, Siemens |
| Models | LKGF1, 10591, L2KGF2, LGCOC10025, LGCOC20025, 482-485, 10381403, LGCOC10026, 10381448, LGCOC20026, 10385387 |
| Date | Oct 26, 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