---
title: "Medtronic, Simplera Sensor, REF: MMT-5100JD1 — FDA record Z-0033-2026 | Is It on Recall"
description: "The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection."
url: https://isitonrecall.com/recall/fda-device-z-0033-2026-medtronic-simplera-sensor-ref-mmt-5100jd1/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Medtronic, Simplera Sensor, REF: MMT-5100JD1 — FDA record Z-0033-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 7, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Medtronic, Simplera Sensor, REF: MMT-5100JD1
- **Reason**: The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.
- **Classification**: Class II
- **Recalling firm**: Medtronic MiniMed, Inc.
- **Quantity**: 1,440 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0033-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0033-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot # HG81GLZ/ GTIN: 20763000649580 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: No distribution OUS: Austria, Belgium, Italy, Spain, Switzerland, United Kingdom

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 8, 2025
- **Recall initiation date**: May 7, 2025
- **Center classification date**: Oct 2, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0033-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic MiniMed, Inc. records](https://isitonrecall.com/brand/medtronic-minimed-inc/)