International safety notice
Recall/Corrective action or ACCELERATOR APS Centrifuge Module, Abbott
Germany / BfArM · DEU · Oct 9, 2008
Key facts
| Title | Recall/Corrective action or ACCELERATOR APS Centrifuge Module, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall/Corrective action or ACCELERATOR APS Centrifuge Module, Abbott |
| Manufacturer | Recall/Corrective action or ACCELERATOR APS Centrifuge Module, Abbott |
| Models | 21.06, FA09SEP2008, 28.99, も9コ0菱言U-亡を朝, U山の-10のLIOコ0トUEの0, 」0」0←, 一」Qココを2亡, 、ON一2に9の, 」Qココを2仁2当0, 07L02-01, UOMN003SVB, 」0」0一 and 8 more |
| Date | Oct 9, 2008 |
| 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