International safety notice
Corrective action for Liaison® Control Biotrin Parvovirus B19 IgM, Diasorin
Germany / BfArM · DEU · Jan 20, 2014
Key facts
| Title | Corrective action for Liaison® Control Biotrin Parvovirus B19 IgM, Diasorin |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Liaison® Control Biotrin Parvovirus B19 IgM, Diasorin |
| Manufacturer | Corrective action for Liaison® Control Biotrin Parvovirus B19 IgM, Diasorin |
| Models | 130012X, 13001, 0.0-0.5, 317011, 0.0-0.3, 0161.487628, 39.0161.487.849, 130012X.130012X, 2014JÖR, 487093, 0161.487093, 130010X and 2 more |
| Date | Jan 20, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 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