International safety notice
Corrective Action for UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 800, Unicel DxC 800 PRO, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i, Beckman Coulter
Germany / BfArM · DEU · Feb 5, 2010
Key facts
| Title | Corrective Action for UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 800, Unicel DxC 800 PRO, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 800, Unicel DxC 800 PRO, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i, Beckman Coulter |
| Manufacturer | Corrective Action for UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 800, Unicel DxC 800 PRO, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i, Beckman Coulter |
| Models | DXC860I, A32319, 664090, UNICE1, 657133 |
| Date | Feb 5, 2010 |
| 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