International safety notice
EUROIMMUN Medizinische Labordiagnostika AG
United Kingdom / MHRA · GBR · Apr 7, 2020
Key facts
| Title | EUROIMMUN Medizinische Labordiagnostika AG |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Anti-Parvovirus B19 ELISA (IgM) |
| Manufacturer | EUROIMMUN Medizinische Labordiagnostika AG |
| Models | 23560, 23911, 2580-9601, 23121, E190626AH, 25855 |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Apr 7, 2020 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 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