International safety notice
Recall for HemosIL von Willebrand Factor Activity, Instrumentation Laboratory
Germany / BfArM · DEU · Apr 24, 2012
Key facts
| Title | Recall for HemosIL von Willebrand Factor Activity, Instrumentation Laboratory |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | HemosIL von Willebrand Factor Activity, Instrumentation Laboratory |
| Manufacturer | Recall for HemosIL von Willebrand Factor Activity, Instrumentation Laboratory |
| Models | B11687, B11498, 0020004700, B11655, B01424 |
| Date | Apr 24, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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