International safety notice
Recall for IMMULITE 2000/2500 Chemiluminescent Substrate Lots L2SUBX 253, 254, 255, 256A, 257A, 258, 259A, Siemens Healthcare Diagnostics
Germany / BfArM · DEU · Jun 16, 2009
Key facts
| Title | Recall for IMMULITE 2000/2500 Chemiluminescent Substrate Lots L2SUBX 253, 254, 255, 256A, 257A, 258, 259A, Siemens Healthcare Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE 2000/2500 Chemiluminescent Substrate Lots L2SUBX 253, 254, 255, 256A, 257A, 258, 259A, Siemens Healthcare Diagnostics |
| Manufacturer | Recall for IMMULITE 2000/2500 Chemiluminescent Substrate Lots L2SUBX 253, 254, 255, 256A, 257A, 258, 259A, Siemens Healthcare Diagnostics |
| Models | L2SUBX259A, L2SUBX253, 0.5—1.8, L2SUBX, L2SUBX256A, L2SUBX254, 2009-05, 973.927.2828, L2SUBX255, L2SUBX258, L2SUBM, L2SUBX257A and 1 more |
| Date | Jun 16, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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