International safety notice
Corrective Action of Siemens for IMMULITE / IMMULITE 1000 Insulin and IMMULITE 2000 / IMMULITE 2000 XPi, Siemens
Germany / BfArM · DEU · May 29, 2012
Key facts
| Title | Corrective Action of Siemens for IMMULITE / IMMULITE 1000 Insulin and IMMULITE 2000 / IMMULITE 2000 XPi, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE / IMMULITE 1000 Insulin and IMMULITE 2000 / IMMULITE 2000 XPi, Siemens |
| Manufacturer | Corrective Action of Siemens for IMMULITE / IMMULITE 1000 Insulin and IMMULITE 2000 / IMMULITE 2000 XPi, Siemens |
| Models | 10381455, L2KIN2, 10381456, 10591, LKIN1, L2KIN6, 10381429 |
| Date | May 29, 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