International safety notice
Corrective action and recall for the Cystic Fibrosis v3 Genotype Assay from Celera Diagnostics
Germany / BfArM · DEU · Oct 24, 2006
Key facts
| Title | Corrective action and recall for the Cystic Fibrosis v3 Genotype Assay from Celera Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Cystic Fibrosis v3 Genotype Assay from Celera Diagnostics |
| Manufacturer | Corrective action and recall for the Cystic Fibrosis v3 Genotype Assay from Celera Diagnostics |
| Models | 04J92-65, V3.5.1, V3.51, FA-CAM-JUL2006-009, 3.5.1, 60018-3315, 5000263, 4J92-66 |
| Date | Oct 24, 2006 |
| 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