International safety notice
Urgent Field Safety Notice for Verigene Gram Positive Blood, Verigene Gram Negative Blood Culture, Verigene Gram Negative Blood Culture V2, Verigene RP Flex, and Vergiene Enteric Pathogens, Verigene CDF by Luminex Corporation US
Germany / BfArM · DEU · Feb 18, 2021
Key facts
| Title | Urgent Field Safety Notice for Verigene Gram Positive Blood, Verigene Gram Negative Blood Culture, Verigene Gram Negative Blood Culture V2, Verigene RP Flex, and Vergiene Enteric Pathogens, Verigene CDF by Luminex Corporation US |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Verigene Gram Positive Blood, Verigene Gram Negative Blood Culture, Verigene Gram Negative Blood Culture V2, Verigene RP Flex, and Vergiene Enteric Pathogens, Verigene CDF |
| Manufacturer | Luminex Corporation US |
| Models | 12212, BC-GNV2, 20-005-023, 20-005-022, 1.512.381.4397, 1.877.785.2323, 512.219.5114, 20-005-026, 1-877-785-2323, 20-005-018, CAN-0269, 20-005-021 and 3 more |
| Date | Feb 18, 2021 |
| 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