Medtronic recalls certain Pocket Adaptor Kits for Deep Brain Stimulation due to incorrect Use-By-Dates on labels. Affected kits include specific model numbers and lot numbers.
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Medtronic is recalling a limited number of Pocket Adaptor Kits for Deep Brain Stimulation (Model 64001 and 64002) because they have incorrect Use-By-Dates on the labels. This could lead to improper use of the device if the dates are not accurate.
The recalled Pocket Adaptor Kits have incorrect Use-By-Dates labeled on them. This means the expiration dates might not be accurate, potentially leading to improper use of the device if the dates are not correctly followed.
Patients with deep brain stimulation devices for parkinsonian tremor who own the recalled Pocket Adaptor Kits. Those with the specific model numbers and lot numbers listed in the recall are most at risk.
Check for the model numbers 64001 or 64002 and the specific lot numbers listed in the recall, such as VA368G3, VA36V7T, VA3347Y, and others. The kits are part of Medtronic's Deep Brain Stimulation system for parkinsonian tremor.
Look for the model numbers 64001 or 64002 and the specific lot numbers listed in the recall to determine if your kit is affected.
The recalled Pocket Adaptor Kits have incorrect Use-By-Dates labeled on them, which could lead to improper use of the device if the dates are not accurately followed.
Check the model numbers and lot numbers listed in the recall to see if your kit is affected. If it is, you should contact Medtronic for further instructions.
The recall indicates that the incorrect dates could lead to improper use of the device, but the hazard is low risk as the issue does not involve immediate danger or injury.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2241-2026 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2241-2026 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
