International safety notice
Recall for Dimension Vista B2-Microglobulin Flex reagent cartridge, Siemens
Germany / BfArM · DEU · Jul 15, 2009
Key facts
| Title | Recall for Dimension Vista B2-Microglobulin Flex reagent cartridge, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Dimension Vista B2-Microglobulin Flex reagent cartridge, Siemens |
| Manufacturer | Recall for Dimension Vista B2-Microglobulin Flex reagent cartridge, Siemens |
| Models | GPF-003-6, 09029MA, 2009-05-20, B2MLC, K7024, BR-08209, 2009-01-19, 35041, B2-MICROGLOBUIIN |
| Date | Jul 15, 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