International safety notice
Enlargement of Corrective Action / Recall for UniCel DxI 600 Systems, UniCel DxI 800 Systems, UniCel DxC 880i Systems, Beckman Coulter
Germany / BfArM · DEU · Aug 12, 2008
Key facts
| Title | Enlargement of Corrective Action / Recall for UniCel DxI 600 Systems, UniCel DxI 800 Systems, UniCel DxC 880i Systems, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | UniCel DxI 600 Systems, UniCel DxI 800 Systems, UniCel DxC 880i Systems, Beckman Coulter |
| Manufacturer | Enlargement of Corrective Action / Recall for UniCel DxI 600 Systems, UniCel DxI 800 Systems, UniCel DxC 880i Systems, Beckman Coulter |
| Models | PCA-C•F-1022-1, PCA-C-F.1022-1, 800-854-3633, A34468, 01-010341-1, 2125A, PCA.C-F-1022-1, PCA-C-F-J022-1, 22454201, 81910, 12.00, PCA-C-F-J022-J and 5 more |
| Date | Aug 12, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching catalog numbers 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