International safety notice
Recall and corrective action of BioMerieux for Vitek 2 GN ID Test Kits
Germany / BfArM · DEU · Oct 14, 2005
Key facts
| Title | Recall and corrective action of BioMerieux for Vitek 2 GN ID Test Kits |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Vitek 2 GN ID Test Kits |
| Manufacturer | Recall and corrective action of BioMerieux for Vitek 2 GN ID Test Kits |
| Models | 21341, 514455-1 |
| Date | Oct 14, 2005 |
| 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