International safety notice
Corrective action for the UniCel DxI Access Immunoassay System with UniCel DxI 800 Modification (MOD ID 10027) and/or UniCel 800 Modification (MOD ID 6733) from Beckman Coulter
Germany / BfArM · DEU · Oct 26, 2007
Key facts
| Title | Corrective action for the UniCel DxI Access Immunoassay System with UniCel DxI 800 Modification (MOD ID 10027) and/or UniCel 800 Modification (MOD ID 6733) from Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the UniCel DxI Access Immunoassay System with UniCel DxI 800 Modification (MOD ID 10027) and/or UniCel 800 Modification (MOD ID 6733) from Beckman Coulter |
| Manufacturer | Corrective action for the UniCel DxI Access Immunoassay System with UniCel DxI 800 Modification (MOD ID 10027) and/or UniCel 800 Modification (MOD ID 6733) from Beckman Coulter |
| Models | 973100, PCA-C-E-1048, 10027, 448-484B, 1-800-854-3633, 55318-1084 |
| Date | Oct 26, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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