International safety notice
Corrective action of the Coulter GENOS Hematology Analyzers from Beckman Coulter
Germany / BfArM · DEU · May 10, 2007
Key facts
| Title | Corrective action of the Coulter GENOS Hematology Analyzers from Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of the Coulter GENOS Hematology Analyzers from Beckman Coulter |
| Manufacturer | Corrective action of the Coulter GENOS Hematology Analyzers from Beckman Coulter |
| Models | 147TH, PCA-M.E-1D18, 526-6932, TOIDEF4, 33196-2500, 33116-9015, 526-7694, 169015, 1-800-526-7694, 11800, 327-6531, RC5PNSE |
| Date | May 10, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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