International safety notice
Recall of Diamed Diagnostika for ID-Heparin/PF4 Antibody Test
Germany / BfArM · DEU · Jun 1, 2005
Key facts
| Title | Recall of Diamed Diagnostika for ID-Heparin/PF4 Antibody Test |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ID-Heparin/PF4 Antibody Test |
| Manufacturer | Recall of Diamed Diagnostika for ID-Heparin/PF4 Antibody Test |
| Models | 050051, 02800.23.10, 64625, 02800.24.10, 45580.28.01, 64602, 050021 |
| Date | Jun 1, 2005 |
| 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