International safety notice
Corrective action for the CXP software versions 1.0, 1.1 and 2.0, Beckman Coulter
Germany / BfArM · DEU · Dec 16, 2004
Key facts
| Title | Corrective action for the CXP software versions 1.0, 1.1 and 2.0, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the CXP software versions 1.0, 1.1 and 2.0, Beckman Coulter |
| Manufacturer | Corrective action for the CXP software versions 1.0, 1.1 and 2.0, Beckman Coulter |
| Models | 123456, D-47704, D-47807, 00000004, 0000000 |
| Date | Dec 16, 2004 |
| 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