Medtronic recalls Minimed Model 503 Remote Transmitters for potential security risks with insulin pumps. Affected units may have vulnerabilities that could compromise patient safety.
There is a potential security vulnerability related to the use of the remote controller accessories with the insulin pumps.
Medtronic is recalling Minimed Model 503 Remote Transmitters used with their insulin pumps due to a potential security vulnerability. This could allow unauthorized access to insulin delivery settings, risking patient safety.
The security vulnerability could allow unauthorized access to insulin pump settings. This might lead to incorrect insulin dosing or other safety issues if someone gains access to the device.
People using Medtronic's MiniMed Paradigm insulin pumps with the Model 503 Remote Transmitter are affected. Those with diabetes who rely on these devices are most at risk.
Check for the Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US) with the MiniMed Paradigm insulin pump. All units have specific serial numbers.
Identify the serial number on your insulin pump to confirm if it's affected.
The recall states there is a potential security vulnerability, but it does not specify if this has caused injuries or serious harm.
Check the serial number on your insulin pump. Affected units are those with the Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US) used with the MiniMed Paradigm insulin pump.
The recall does not specify a remedy, so you should contact Medtronic directly for guidance.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0178-2020 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0178-2020 from Medtronic. 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.
