Medtronic recalls 1x4 Pocket Adaptor Kits for Deep Brain Stimulation with incorrect Use-By-Dates. Model 64001 and 64002 kits have specific lot numbers and GTINs listed in the recall.
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 1x4 Pocket Adaptor Kits for Deep Brain Stimulation (Model 64001 and 64002) due to incorrect Use-By-Dates on the packaging. This issue does not pose a safety risk to users but may affect the product's shelf life and compliance with medical regulations.
The recalled kits have incorrect Use-By-Dates printed on the packaging. This means the product may expire before the intended use date, potentially leading to compliance issues with medical regulations. However, the hazard does not involve immediate safety risks like injury or malfunction.
Patients with deep brain stimulation devices for parkinsonian tremor who own the recalled 1x4 Pocket Adaptor Kits (Model 64001 and 64002) with specific lot numbers and GTINs listed in the recall are most at risk.
Check for the product name 'Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation', model numbers 64001 or 64002, and specific lot numbers or GTINs listed in the recall details.
Review the product's model number and lot number to confirm if it matches the recalled items listed in the official notice.
No, the recall is for incorrect Use-By-Dates on the packaging, which does not pose a safety risk. The hazard is related to product expiration and regulatory compliance, not immediate injury or malfunction.
Check for the product name 'Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation', model numbers 64001 or 64002, and specific lot numbers or GTINs listed in the recall details.
The recall does not require immediate action. However, you should check the product details to confirm if it is recalled and contact Medtronic if you have concerns.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2240-2026 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2240-2026 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.
