International safety notice
Recall for Captia VZV IgM Kit, Trinity Biotech
Germany / BfArM · DEU · Aug 31, 2010
Key facts
| Title | Recall for Captia VZV IgM Kit, Trinity Biotech |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Captia VZV IgM Kit, Trinity Biotech |
| Manufacturer | Recall for Captia VZV IgM Kit, Trinity Biotech |
| Models | 2769888, 2325650, 35312769888, 239206, 35312769800 |
| Date | Aug 31, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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