International safety notice
Recall and corrective action of Dade Behring for Coagulation Factor VIII Deficient Plasma
Germany / BfArM · DEU · Jul 27, 2005
Key facts
| Title | Recall and corrective action of Dade Behring for Coagulation Factor VIII Deficient Plasma |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coagulation Factor VIII Deficient Plasma |
| Manufacturer | Recall and corrective action of Dade Behring for Coagulation Factor VIII Deficient Plasma |
| Models | 503859B, 394594, 5038470, 503849E, B4219-1, 503848A, BR.17405, 06421-39, 503858A, BR-17305, 503846A, 34219-11 and 20 more |
| Date | Jul 27, 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