International safety notice
Corrective Action for Coulter LH 500 Analyzer, Coulter LH 750 Analyzer, Coulter LH 780 Analyzer, Coulter GEN*S Analyzer and UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter
Germany / BfArM · DEU · Mar 17, 2010
Key facts
| Title | Corrective Action for Coulter LH 500 Analyzer, Coulter LH 750 Analyzer, Coulter LH 780 Analyzer, Coulter GEN*S Analyzer and UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter LH 500 Analyzer, Coulter LH 750 Analyzer, Coulter LH 780 Analyzer, Coulter GEN*S Analyzer and UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
| Manufacturer | Corrective Action for Coulter LH 500 Analyzer, Coulter LH 750 Analyzer, Coulter LH 780 Analyzer, Coulter GEN*S Analyzer and UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
| Models | 800-526-7694, QUALT6, 123456, PCA-13012.C, $123456, 11800, ANALYS18, UNLCE10, PCA-F3012, 123453 |
| Date | Mar 17, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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