Medtronic recalls Paradigm insulin pumps (MMT-712E) due to wireless cybersecurity risks that could allow unauthorized access to 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 its Paradigm insulin pumps with model number MMT-712E because of potential cybersecurity vulnerabilities. This could let unauthorized users remotely change insulin settings, risking serious health consequences.
The pumps use wireless radio frequency to communicate, which could be exploited by unauthorized users. This allows someone to remotely adjust insulin delivery settings without the user's knowledge, potentially causing dangerous blood sugar levels.
People using Medtronic MiniMed Paradigm insulin pumps with model MMT-712E are affected. Those with diabetes who rely on these pumps are most at risk.
Check for the model number MMT-712E on your insulin pump. The pumps were sold outside the US with all software versions available.
Identify your pump's model number to confirm if it's MMT-712E.
Reach out to Medtronic MiniMed for guidance on securing your pump or potential next steps.
No, the recall applies only to pumps sold outside the US with all software versions.
The official recall does not specify security steps; contact Medtronic for guidance.
The recall does not require immediate stoppage; contact Medtronic for next steps.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1585-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1585-2020 from Medtronic 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
