FDANovember 21, 2024device

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B

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

UPCs

0064316989094700763000447090

Recall history

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

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SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B — Recall Details · AllClear