International safety notice
St. Jude Medical
United Kingdom / MHRA · GBR · Aug 18, 2015
Key facts
| Title | St. Jude Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Atrial implantable cardioverter defibrillator |
| Manufacturer | St. Jude Medical |
| Models | EX1150 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Aug 18, 2015 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 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