International safety notice
Recall and corrective action of Beckman Coulter for MXP software versions 1.0 and 2.0 for FC500 systems
Germany / BfArM · DEU · Aug 4, 2005
Key facts
| Title | Recall and corrective action of Beckman Coulter for MXP software versions 1.0 and 2.0 for FC500 systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FC500 systems |
| Manufacturer | Recall and corrective action of Beckman Coulter for MXP software versions 1.0 and 2.0 for FC500 systems |
| Models | 327-6531, •169015, 06.2005, 800-526-7694, 33H6„9015, 147TH, PCA.M-C-1052, 3800800, 33196-2500 |
| Date | Aug 4, 2005 |
| 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