Medtronic recalls Simplera Sensor model MMT-5100JD1 due to potential infection from cap label not adhering to the sensor. Affected units sold with lot # HG81GLZ and GTIN 20763000649580.
The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.
Medtronic is recalling Simplera Sensor devices with model number MMT-5100JD1 because the cap label might not stick properly, which could lead to infection. This is a safety issue for people using medical devices that require sterile conditions.
The cap label on the sensor may not stay securely attached, which can compromise the sensor's sterility. This increases the risk of infection because medical devices need to be kept sterile to prevent contamination.
People with Medtronic Simplera Sensor devices (model MMT-5100JD1) who use the device for medical purposes are most at risk. The recall affects specific units sold with lot number HG81GLZ and GTIN 20763000649580.
Check for the model number MMT-5100JD1 on the device. Affected units were sold with lot number HG81GLZ and GTIN 20763000649580.
Look for the model number MMT-5100JD1 and lot number HG81GLZ on the device.
The recall states the cap label may not adhere properly, which could increase infection risk. However, the remedy is not stated in the record, so no specific action is required beyond checking the label.
Check for the model number MMT-5100JD1 and lot number HG81GLZ on the device. Affected units were sold with GTIN 20763000649580.
The recall record does not specify a remedy, so no action is required beyond checking the device label for the model and lot numbers.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0033-2026 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0033-2026 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.
