Medtronic recalls Paradigm insulin pumps (MMT-722K) due to wireless cybersecurity risks allowing unauthorized insulin delivery changes. Affected users should contact Medtronic for security updates.
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-722K because of potential cybersecurity vulnerabilities. These pumps could be hacked to change insulin settings remotely, risking serious health consequences if an unauthorized person accesses the device.
The pumps use wireless radio frequency to communicate, which could allow hackers to connect remotely and alter insulin delivery settings. This might lead to incorrect insulin dosing if an unauthorized person changes the pump's settings.
People using Medtronic MiniMed Paradigm insulin pumps with model number MMT-722K are affected. Those with diabetes who rely on these pumps for insulin delivery are most at risk.
Check if your insulin pump has the model number MMT-722K. The recall applies to all software versions of this specific pump model.
Reach out to Medtronic for security updates or to get instructions on securing your pump.
No, this recall specifically affects Medtronic MiniMed Paradigm pumps with model number MMT-722K.
Check the model number on your pump; if it's MMT-722K, you're affected.
The recall does not require immediate stoppage; contact Medtronic for security updates.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1590-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1590-2020 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.
