FDAJuly 26, 2022device

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.

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

The hazard

Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of the Vanta Implantable Neurostimulator (INS) Model 977006.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

Recall history

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

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