International safety notice
Corrective Action for IMMULITE / IMMULITE 1000 Third Generation TSH, IMMULITE 2000 Rapid TSH / IMMULITE 2000 XPi Rapid TSH and IMMULITE 2500 Rapid TSH, Siemens
Germany / BfArM · DEU · Jul 16, 2012
Key facts
| Title | Corrective Action for IMMULITE / IMMULITE 1000 Third Generation TSH, IMMULITE 2000 Rapid TSH / IMMULITE 2000 XPi Rapid TSH and IMMULITE 2500 Rapid TSH, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE / IMMULITE 1000 Third Generation TSH, IMMULITE 2000 Rapid TSH / IMMULITE 2000 XPi Rapid TSH and IMMULITE 2500 Rapid TSH, Siemens |
| Manufacturer | Corrective Action for IMMULITE / IMMULITE 1000 Third Generation TSH, IMMULITE 2000 Rapid TSH / IMMULITE 2000 XPi Rapid TSH and IMMULITE 2500 Rapid TSH, Siemens |
| Models | L5KRT2, LKTS1, L2KRT2, 10591 |
| Date | Jul 16, 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