Medtronic MiniMed Paradigm Veo insulin pumps with model numbers MMT-554CM and MMT-754CM (software versions 2.7A or lower) are recalled due to potential cybersecurity vulnerabilities that could allow 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 MiniMed Paradigm Veo insulin pumps with model numbers MMT-554CM and MMT-754CM and software versions 2.7A or lower are being recalled. This recall is due to potential cybersecurity vulnerabilities that could allow unauthorized users to remotely change insulin settings and delivery.
The insulin pumps have wireless radio frequency communication that could be exploited by unauthorized users to remotely change insulin settings and delivery. This could lead to unintended insulin doses or disruptions in treatment without the user's knowledge.
People who own or use Medtronic MiniMed Paradigm Veo insulin pumps with model numbers MMT-554CM or MMT-754CM and software versions 2.7A or lower are affected. Those with diabetes who rely on these pumps are at the highest risk.
Check your insulin pump's model number on the device or packaging. The affected models are MMT-554CM and MMT-754CM with software versions 2.7A or lower. These pumps are only available outside the US.
Identify your insulin pump's model number to see if it matches MMT-554CM or MMT-754CM.
Reach out to Medtronic MiniMed for guidance on next steps if your pump is affected.
No, these pumps are only available outside the US.
Software versions 2.7A or lower.
Check the model number on the pump or packaging; affected models are MMT-554CM and MMT-754CM with software versions 2.7A or lower.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1596-2020 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1596-2020 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.
