FDADecember 19, 2023device

Model A710 Intellis Clinician Programmer Application, version 2.0.97

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

The hazard

Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00763000520076

Recall history

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

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