International safety notice
Urgent Field Safety Notice for VITEK 2 ID / AST Card Types by bioMérieux Inc
Germany / BfArM · DEU · Jan 31, 2019
Key facts
| Title | Urgent Field Safety Notice for VITEK 2 ID / AST Card Types by bioMérieux Inc |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VITEK 2 ID / AST Card Types |
| Manufacturer | bioMérieux Inc |
| Models | AST-N275, 2410636203, 5930821203, 16-FEB-20, 28-AUG-18, 22-AUG-18, 413753, 29AUG2018, 7430809203, 15-AUG-18, AST-P612, 421040 and 151 more |
| Date | Jan 31, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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