Medtronic recalls Paradigm insulin pumps (MMT-522K) due to wireless cybersecurity risks that could allow unauthorized access to insulin delivery 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-522K because they have wireless security flaws that could let hackers change insulin settings. This could lead to dangerous insulin delivery changes if someone gains access to the pump.
The pumps use wireless radio frequency to communicate, which could be exploited by unauthorized users to change insulin delivery settings. This might cause incorrect insulin dosing if hackers alter the pump's programming.
People using Medtronic MiniMed Paradigm insulin pumps with model number MMT-522K are affected. Those with diabetes who rely on these pumps are most at risk.
Check for the model number MMT-522K on your insulin pump. The recall applies to all software versions of this specific pump model.
Look for the model number MMT-522K on your insulin pump to confirm if it is affected.
Reach out to Medtronic MiniMed directly for guidance on next steps and potential remedies.
The recall indicates potential cybersecurity risks, but the pump is not inherently unsafe. Users should follow the recommended actions to mitigate risks.
Check the model number on your pump; affected units are Medtronic MiniMed Paradigm pumps with model number MMT-522K.
Contact Medtronic MiniMed directly for specific instructions on how to proceed with 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-1589-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1589-2020 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.
