International safety notice
Corrective action for Siemens Factor VIII chromogenic assay on CS Series Automated Blood Coagulation Analyzers, Sysmex
Germany / BfArM · DEU · Apr 24, 2014
Key facts
| Title | Corrective action for Siemens Factor VIII chromogenic assay on CS Series Automated Blood Coagulation Analyzers, Sysmex |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Siemens Factor VIII chromogenic assay on CS Series Automated Blood Coagulation Analyzers, Sysmex |
| Manufacturer | Corrective action for Siemens Factor VIII chromogenic assay on CS Series Automated Blood Coagulation Analyzers, Sysmex |
| Models | 2000I, GPF-003, CS-2000I, GP-003, 10488583, CS-2100I, CS-5100, 2013-12-31, 10713586, CS2000I, BR-02314, 10488585 |
| Date | Apr 24, 2014 |
| 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