International safety notice
Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700
Germany / BfArM · DEU · Aug 17, 2005
Key facts
| Title | Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700 |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the software of Olympus systems AU400, AQU640 and AU2700 |
| Manufacturer | Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700 |
| Models | AU5400, AU400, 21.07.2005, 23773, D-20034, AU640, AU600, AU2700 |
| Date | Aug 17, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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