International safety notice
Urgent Safety Notice for the Omnis system, Dako Denmark A/S
Germany / BfArM · DEU · Jul 13, 2015
Key facts
| Title | Urgent Safety Notice for the Omnis system, Dako Denmark A/S |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Omnis system, Dako Denmark A/S |
| Manufacturer | Urgent Safety Notice for the Omnis system, Dako Denmark A/S |
| Models | 1.4.0, TX30078, 00509, 1.3.0, CAPA00509 |
| Date | Jul 13, 2015 |
| 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