Medtronic recalls Paradigm insulin pumps (MMT-723, software 2.4A or lower) due to wireless cybersecurity risks that could allow unauthorized insulin delivery changes.
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-723 and software version 2.4A or lower 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 insulin pumps use wireless radio frequency to communicate, which could be exploited by unauthorized users to remotely change settings and control insulin delivery. This might cause incorrect insulin doses without the user's knowledge, potentially leading to dangerous blood sugar levels.
People using Medtronic MiniMed Paradigm insulin pumps with model MMT-723 and software version 2.4A or lower are affected. Those with diabetes who rely on these pumps for insulin delivery are most at risk.
Check if your pump has the model number MMT-723 and software version 2.4A or lower. The recall covers all units sold with these specifications.
Install the latest software version from Medtronic to fix the security vulnerability.
No, only the Paradigm insulin pumps with model number MMT-723 and software version 2.4A or lower are affected.
Check your pump's model number and software version; the recall covers MMT-723 pumps with software version 2.4A or lower.
No, but you should update the software to the latest version to address the security vulnerability.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1594-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1594-2020 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.
