International safety notice
Recall of Beckman Coulter for the automated pipetting protocol Dil-AFP
Germany / BfArM · DEU · Aug 19, 2005
Key facts
| Title | Recall of Beckman Coulter for the automated pipetting protocol Dil-AFP |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the automated pipetting protocol Dil-AFP |
| Manufacturer | Recall of Beckman Coulter for the automated pipetting protocol Dil-AFP |
| Models | ACCESSØ2, 448-4848, 1-800-854-3633, PCA-C-C-1055, 55318-1084 |
| Date | Aug 19, 2005 |
| 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