International safety notice
Medtronic Mosaic Aortic Bioprosthesis
Swiss / SwissMedic · CHE · Jan 20, 2014
Key facts
| Title | Medtronic Mosaic Aortic Bioprosthesis |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | Medtronic Mosaic Aortic Bioprosthesis |
| Manufacturer | Medtronic Inc. |
| Models | CH-3053, FA599, 1.000 |
| Event type | Safety Notice |
| Date | Jan 20, 2014 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes 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