International safety notice
Corrective action for Total IgE on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens
Germany / BfArM · DEU · Jan 16, 2014
Key facts
| Title | Corrective action for Total IgE on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Total IgE on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens |
| Manufacturer | Corrective action for Total IgE on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens |
| Models | 1.495, NVF1JLITEMVMIJLITE, 10380873, 278.125, IECA1, N.N.1ULITE, 79.81, 509.81, 2.745, MNVF1JLITE, L2KIE2, NVF1JLITE and 13 more |
| Date | Jan 16, 2014 |
| 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