International safety notice
Batch recall of ORG 908MX Anti Mumps Virus IgM, ORGENTEC Diagnostika GmbH
Germany / BfArM · DEU · Oct 19, 2016
Key facts
| Title | Batch recall of ORG 908MX Anti Mumps Virus IgM, ORGENTEC Diagnostika GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of ORG 908MX Anti Mumps Virus IgM, ORGENTEC Diagnostika GmbH |
| Manufacturer | Batch recall of ORG 908MX Anti Mumps Virus IgM, ORGENTEC Diagnostika GmbH |
| Models | 5513A, 55134, 908MX, 100352, 1605848 |
| Date | Oct 19, 2016 |
| 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