Medtronic recalls MiniMed MMT-508 insulin pumps due to wireless security risks that could allow unauthorized access to change insulin settings.
The action is being initiated due to potential cybersecurity vulnerabilities related to a series of insulin pumps that are designed to communicate using a wireless radio frequency (RF). An unauthorized person could potentially connect wirelessly to a nearby insulin pump to change settings and control insulin delivery.
Medtronic is recalling all MiniMed MMT-508 insulin pumps because they have wireless security flaws that could let hackers change insulin settings remotely. This could lead to dangerous insulin delivery changes without the user's knowledge.
The pumps use wireless radio frequency to communicate, which could be exploited by unauthorized users to remotely change insulin settings. This might cause incorrect insulin delivery, leading to dangerous blood sugar levels.
People using Medtronic MiniMed MMT-508 insulin pumps are affected. Those with diabetes who rely on these pumps for insulin delivery are most at risk.
Check for the model number MMT-508 on the pump's label. The recall covers all software versions of this pump model.
Review your pump's current settings to ensure insulin delivery is functioning correctly.
Contact Medtronic to get the latest software updates for your pump.
No, this recall specifically affects MiniMed MMT-508 insulin pumps with all software versions.
Check the model number on your pump's label; if it's MMT-508, it's affected.
Contact Medtronic to update your software or get guidance on securing your pump.
We’ve drafted a message you can send Medtr: MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1581-2020 — Medtr: MiniMed Medtr: MiniMed Hello, I own a Medtr: MiniMed that is covered by recall Z-1581-2020 from Medtr: MiniMed. 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.
