Medtronic recalls all Paradigm 512 insulin pumps 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 is recalling all Paradigm 512 insulin pumps because they have cybersecurity flaws that could let hackers remotely change insulin settings. This poses a risk of incorrect insulin delivery, which could lead to dangerous health outcomes.
The insulin pump can be hacked remotely via wireless signals, allowing unauthorized users to adjust insulin delivery settings. This could cause incorrect insulin dosing, leading to hypoglycemia or hyperglycemia. The risk is active but not immediate unless the pump is connected to a hacker.
People with diabetes who use the MiniMed Paradigm 512 insulin pump are affected. Those with the pump's software version listed in the recall are at the highest risk.
Check if your insulin pump has the brand Medtronic MiniMed and model Paradigm 512. The recall applies to all software versions of this pump.
Identify your pump's model and software version to confirm if it is affected by the recall.
Reach out to Medtronic MiniMed for guidance on next steps if your pump is affected.
Yes, the recall applies to all software versions of the MiniMed Paradigm 512 insulin pump.
Hackers could connect wirelessly to the pump using radio frequency signals to change insulin settings remotely.
Check your pump's model and software version, then contact Medtronic MiniMed for specific instructions.
We’ve drafted a message you can send Medtr: a short, human brand name for headings (e.g. "Trsmima") to request your refund or repair — edit it as you like.
Subject: Recall Z-1583-2020 — Medtr: a short, human brand name for headings (e.g. "Trsmima") Medtr: a short, human brand name for Hello, I own a Medtr: a short, human brand name for headings (e.g. "Trsmima") that is covered by recall Z-1583-2020 from Medtr: a short, human brand name for headings (e.g. "Trsmima"). 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.
