International safety notice
Medtronic FA 949
United Kingdom / MHRA · GBR · Dec 1, 2020
Key facts
| Title | Medtronic FA 949 |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Intellis Clinician Programmer Application |
| Manufacturer | Medtronic FA 949 |
| Models | 1.3.80, 212213, 01923, 1.3.130, FA949, CT900, V1.3.130 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Dec 1, 2020 |
| Regulator page | gov.uk |
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