International safety notice
Medtronic
United Kingdom / MHRA · GBR · Sep 1, 2019
Key facts
| Title | Medtronic |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Euphora Rapid Exchange Balloon Dilatation Catheter / Solarice Rapid Exchange Balloon Dilatation Catheter |
| Manufacturer | Medtronic |
| Models | 217616454, EUP4030X, 217253572, 217777613, 217799248, 217535798, 217602537, SLC3512X, EUP22515X, SLC3510X, 217262908, 217401005 and 787 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Sep 1, 2019 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 10–99 Matching device models 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