FDAFebruary 15, 2025device

Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067040725 REF LSP112V UDI-DI code: 05415067034472 The Aveir leadless pacemaker system supports the implantation and use of an Aveir Leadless Pacemaker (LP) within the targeted chamber(s) of the heart for monitoring ...

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

The hazard

Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.

What to do

FDA enforcement status: Ongoing

Brands named

abbott medicalabbott

UPCs

0541506704072505415067034472

Recall history

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

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