Medtronic recalls Paradigm insulin pumps (MMT-722) due to wireless cybersecurity risks allowing unauthorized remote control of insulin delivery.
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-722 because they have wireless cybersecurity vulnerabilities. This could let hackers remotely change insulin settings, risking dangerous insulin levels for users.
The pumps use wireless radio frequency to communicate, which could be exploited by unauthorized users to connect remotely. This might allow hackers to change insulin delivery settings without the user's knowledge, potentially causing dangerous blood sugar levels.
People using Medtronic MiniMed Paradigm insulin pumps with model number MMT-722 are affected. Those with diabetes who rely on these pumps for insulin delivery are at risk of unsafe insulin adjustments.
Check if your insulin pump has the model number MMT-722. The recall covers all software versions of this specific pump model.
Identify your insulin pump's model number to confirm if it's MMT-722.
Reach out to Medtronic MiniMed for guidance on next steps and potential remedies.
The recall does not require immediate discontinuation; users should check their pump model and contact Medtronic for guidance.
This is a cybersecurity issue that could allow unauthorized remote control of insulin delivery settings.
Check if your pump has the model number MMT-722; all software versions of this model are included in the recall.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1588-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1588-2020 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.
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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.
