International safety notice
Corrective action for Human IgM Kit for use on SPA PLUS, Binding Site
Germany / BfArM · DEU · Dec 23, 2013
Key facts
| Title | Corrective action for Human IgM Kit for use on SPA PLUS, Binding Site |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | use on SPA PLUS, Binding Site |
| Manufacturer | Corrective action for Human IgM Kit for use on SPA PLUS, Binding Site |
| Models | 12580, NK012.S, 56.4G, SIN144, NK012.10S |
| Date | Dec 23, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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