Reported Jun 3, 2026 · Ongoing
Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for…
Medtronic Neuromodulation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Neuromodulation · 7000 Central Ave Ne · Minneapolis, MN · 55432-3568
Is this the product you have?
- Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor
- Lot codes and dates
105 of 105 products
Products covered by this recall Model / number Product as published 00643169090866Lot Number VA368G3 00643169090866Lot Number VA36V7T 00643169936584Lot Number VA3347Y 00643169936584Lot Number VA33481 00643169936584Lot Number VA33M8V 00643169936584Lot Number VA33M92 00643169936584Lot Number VA33T31 00643169936584Lot Number VA33T33 00643169936584Lot Number VA35B5D 00643169936584Lot Number VA35B5E 00643169936584Lot Number VA35WSP 00643169936584Lot Number VA35WSU 00763000963040Lot Number VA35TTU 00763000963040Lot Number VA35TTV 00763000963040Lot Number VA368FZ 00763000963040Lot Number VA368G3 00763000963040Lot Number VA36V7T 00763000963040Lot Number VA36V8Q 00763000968427Lot Number 0231980220 00763000968427Lot Number 0231980221 - Amount recalled
- 275 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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