Medtronic recalls Paradigm insulin pumps (MMT-522) due to wireless cybersecurity risks allowing unauthorized control of insulin delivery. Affected users should contact Medtronic for guidance.
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-522 because of potential cybersecurity vulnerabilities. These pumps could be hacked to 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 remotely change insulin settings. This might lead to incorrect insulin dosing, causing dangerous blood sugar levels.
People using Medtronic MiniMed Paradigm insulin pumps with model number MMT-522 are affected. Those with diabetes who rely on these pumps for insulin delivery are at the highest risk.
Check for the model number MMT-522 on your insulin pump. The recall applies to all software versions of this specific pump model.
Reach out to Medtronic directly for instructions on securing your pump or updating software.
No, this recall specifically applies to Medtronic MiniMed Paradigm pumps with model number MMT-522.
The recall does not require immediate stoppage, but you should contact Medtronic for guidance on securing your pump.
Look for the model number MMT-522 on your insulin pump. The recall applies to all software versions of this model.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1587-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1587-2020 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.
