International safety notice
Corrective action for IMMULITE 2000/IMMULITE 2000 XPi products, Siemens Healthcare Diagnostics
Germany / BfArM · DEU · Mar 11, 2015
Key facts
| Title | Corrective action for IMMULITE 2000/IMMULITE 2000 XPi products, Siemens Healthcare Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE 2000/IMMULITE 2000 XPi products, Siemens Healthcare Diagnostics |
| Manufacturer | Corrective action for IMMULITE 2000/IMMULITE 2000 XPi products, Siemens Healthcare Diagnostics |
| Models | 19962, 0.989, L2KGI2, 54561, 54560, 19981, 54590, 54581, 54563, 54580, 19982, 10380988 and 18 more |
| Date | Mar 11, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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