International safety notice
Recall and corrective action for FC 500 MPL Flow Cytometry Systems with MXP Software (versions 2.0 and 2.1) from Beckman Coulter
Germany / BfArM · DEU · Jan 25, 2007
Key facts
| Title | Recall and corrective action for FC 500 MPL Flow Cytometry Systems with MXP Software (versions 2.0 and 2.1) from Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FC 500 MPL Flow Cytometry Systems with MXP Software (versions 2.0 and 2.1) from Beckman Coulter |
| Manufacturer | Recall and corrective action for FC 500 MPL Flow Cytometry Systems with MXP Software (versions 2.0 and 2.1) from Beckman Coulter |
| Models | 1-800-526-7694 |
| Date | Jan 25, 2007 |
| 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