Aurora Ev-icd™ Mri Surescan™
Aurora EV-ICD™ MRI SureScan™ Recall Summary Aurora EV-ICD™ MRI SureScan™ implantable cardioverter defibrillators are being recalled across Canada due to a performance issue. The devices are designed to treat abnormal heart rhythms in patients who have received them. This is classified as a Class I recall, which indicates a serious problem.
- Product
- Aurora EV-ICD™ MRI SureScan™
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-11-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8f094611-1feb-4034-9c39-5d5788cb814a