Medtronic MiniMed, Inc. 2025-10-08 Health serious FDA
Health · FDA · Recall #FDA-Z-0033-2026
Medtronic, Simplera Sensor, REF: MMT-5100JD1 Recall
Issued October 8, 2025 · Medtronic MiniMed, Inc.
In October 2025, Medtronic MiniMed, Inc. recalled the Medtronic, Simplera Sensor, REF: MMT-5100JD1, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.
What you should do
- 1 Stop using Medtronic, Simplera Sensor, REF: MMT-5100JD1 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medtronic MiniMed, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Medtronic MiniMed, Inc.
- Category
- Health
- Recall date
- October 8, 2025
- Units affected
- Not reported
- Sold at
- US: No distribution OUS: Austria, Belgium, Italy, Spain, Switzerland, United Kingdom
- Recall number
- FDA-Z-0033-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Medtronic MiniMed, Inc. has 7 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.