International safety notice
Corrective Action/Recall for UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter
Germany / BfArM · DEU · Apr 1, 2010
Key facts
| Title | Corrective Action/Recall for UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
| Manufacturer | Corrective Action/Recall for UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter |
| Models | Q.1ESTIM8, 1.1.2.0, 800-526-7694, 11800, 626-7694, 526-6932, MT6CEDM, 13512, 327-6531, 33196-2500, REPRESENTH9, ACTONRE80LUÜON and 5 more |
| Date | Apr 1, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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