FDADecember 3, 2022device

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A

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

The hazard

Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00643169890923

Recall history

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

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Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A — Recall Details · AllClear