International safety notice
Corrective Action for all Access/Access 2 Immunoassay-Systems, SYNCHRON LXi 725 Clinical-Systems and UniCel DxC 600i SYNCHRON Access Clinical-Systems, Beckman Coulter
Germany / BfArM · DEU · Dec 17, 2013
Key facts
| Title | Corrective Action for all Access/Access 2 Immunoassay-Systems, SYNCHRON LXi 725 Clinical-Systems and UniCel DxC 600i SYNCHRON Access Clinical-Systems, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | all Access/Access 2 Immunoassay-Systems, SYNCHRON LXi 725 Clinical-Systems and UniCel DxC 600i SYNCHRON Access Clinical-Systems, Beckman Coulter |
| Manufacturer | Corrective Action for all Access/Access 2 Immunoassay-Systems, SYNCHRON LXi 725 Clinical-Systems and UniCel DxC 600i SYNCHRON Access Clinical-Systems, Beckman Coulter |
| Date | Dec 17, 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