FDANovember 13, 2023device

Medtronic SynchroMed II, Model 8637-40, Programmable pump

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

The hazard

Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug delivery after leaving the MRI magnetic field, which is inconsistent with the current labeling.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00613994483195006431691008240064316934521800643169345225

Recall history

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

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Medtronic SynchroMed II, Model 8637-40, Programmable pump — Recall Details · AllClear