Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Medtronic Recalled by Medtronic MiniMed, Inc. Due to The device cap label may not adhere to...

Date: May 7, 2025
Company: Medtronic MiniMed, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic MiniMed, Inc. directly.

Affected Products

Medtronic, Simplera Sensor, REF: MMT-5100JD1

Quantity: 1,440 units

Why Was This Recalled?

The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.

Where Was This Sold?

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

About Medtronic MiniMed, Inc.

Medtronic MiniMed, Inc. has 22 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report