Medtronic recalls MiniMed Paradigm insulin pumps (MMT-712) 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 all MiniMed Paradigm insulin pumps with model number MMT-712. This recall is due to potential cybersecurity vulnerabilities that could let hackers remotely adjust insulin settings.
The insulin pump can be hacked via wireless signals to change insulin delivery settings without the user's knowledge. This could lead to dangerous blood sugar levels if insulin is delivered incorrectly.
People using MiniMed Paradigm insulin pumps with model number MMT-712 are affected. Those with diabetes who rely on these pumps are at the highest risk.
Check for the model number MMT-712 on your MiniMed Paradigm insulin pump. The recall applies to all software versions of this model.
Identify the model number on your MiniMed Paradigm insulin pump to confirm if it's MMT-712.
Reach out to Medtronic MiniMed for guidance on next steps for your specific pump model.
No, this recall specifically applies to MiniMed Paradigm insulin pumps with model number MMT-712.
Hackers could connect wirelessly to the pump to change insulin settings without the user's knowledge.
The recall does not require immediate stop use; contact Medtronic for specific guidance.
We’ve drafted a message you can send Medtr: MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1584-2020 — Medtr: MiniMed Medtr: MiniMed Hello, I own a Medtr: MiniMed that is covered by recall Z-1584-2020 from Medtr: 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.
