International safety notice
Corrective action for the IMMULITE® 2000/IMMULITE® 2000 XPi Immunoassay Systems, Siemens Healthcare Diagnostics Inc.
Germany / BfArM · DEU · Jun 10, 2015
Key facts
| Title | Corrective action for the IMMULITE® 2000/IMMULITE® 2000 XPi Immunoassay Systems, Siemens Healthcare Diagnostics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the IMMULITE® 2000/IMMULITE® 2000 XPi Immunoassay Systems, Siemens Healthcare Diagnostics Inc. |
| Manufacturer | Corrective action for the IMMULITE® 2000/IMMULITE® 2000 XPi Immunoassay Systems, Siemens Healthcare Diagnostics Inc. |
| Models | 10290607 |
| Date | Jun 10, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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