FDANovember 21, 2024device

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D

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

The hazard

Software issues were identified in application version 2.x.

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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