FDAJanuary 9, 2025device

A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

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

The hazard

Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00763000632793

Recall history

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

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A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System. — Recall Details · AllClear