FDAMay 15, 2024device

A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0.4648), Version 3.0.x (3.0.1057, 3.0.1062, 3.0.1081, and 3.0.1098), Version 4.0.x (4.0.1052). Includes the below product descriptions: 1. ADAPTOR 64...

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

The hazard

Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are limited to HEAD ONLY MRI eligibility.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

006139945449400061399460447700613994604484006139946044910064316909086600643169936584007630001118470076300011185400763000111861006139945449570061399460444600613994604453

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →