Heartmate III Lvas Implant Ki
HeartMate III LVAS Implant Kit Recall The HeartMate III Left Ventricular Assist System (LVAS) Implant Kit, a mechanical heart pump device, is being recalled across Canada due to a defect that could affect how the device operates. This recall applies to patients who have received or may receive this implant, which is used to support heart function in people with advanced heart failure. The recall is classified as Class I, the most serious category, indicating a potential for serious adverse health consequences.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-06-13
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a9e7a20f-08ed-4333-92ae-4a3daf315747