FDAFebruary 5, 2024device

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.

What to do

FDA enforcement status: Ongoing

Brands named

abbott medicalabbott

UPCs

05415067034472

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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