Official recall record
Amplatzer™ Amulet™ Left Atrial Appendage Occluder
- Issuing authority
- Health Canada
- Alert date
- 2026-09-25
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
The current Amulet™ IFU contains a contraindication against use "where placement of the device would interfere with any intracardiac or intravascular structures." Abbott is updating this contraindication to specifically identify the pulmonary artery as one of the adjacent structures. In addition, Abbott is updating the IFU to include additional guidance about assessing the distance between the device landing zone and the pulmonary artery. Abbott recently completed additional physician training on this subject. For clarification, this recall is not associated with defectiveness or possible defectiveness. Abbott is informing consignees about changes to the instructions for use (IFU) for the Amplatzer™ Amulet™ Left Atrial Appendage Occluder (referred to as Amulet™) regarding pulmonary artery injury (PAI).
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-09-29.