Medtronic MiniMed, Inc. recalls
Every recall we track for Medtronic MiniMed, Inc. — 43 in all, from 2023–2026 — plus the complaints and injury reports the public filed about them. 6 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Medtronic MiniMed, Inc. more than tripled in 2025 (18, up from 3 in 2024). 14% rated “stop using now”.
All FDA recall records for Medtronic MiniMed, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 3 | 0 | 0 | 3 |
| 2025 | 2 | 13 | 3 | 0 | 18 |
| 2026 (to date) | 4 | 16 | 1 | 0 | 21 |
What to do if you have a recalled Medtronic MiniMed, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medtronic MiniMed, Inc. recalls
15 shown- Stop using nowMedical device
Medtronic MiniMed, Inc. recalls Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product
Medtronic recalls MiniMed Flex insulin pumps (MMT-8062/8072) due to failed verification tests that may cause inaccurate insulin delivery or device failure.
MiniMedAug 20, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtronic recalls MiniMed 670G insulin pumps with specific model numbers due to potential cleaning issues causing insulin delivery errors. Affected users should contact Medtronic for details.
Medtr: MiniMedJul 13, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Medtronic MiniMed recalls Go app versions 1.0.0 and 1.1.0 for iOS and Android devices. These versions may not trigger nighttime alerts when certain settings are disabled, risking missed insulin doses and hyperglycemia.
Medtronic MiniMedJun 16, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
Medtronic recalls MiniMed 780G insulin pumps with specific software versions due to a software anomaly that can cause insulin delivery to stop when paired with Instinct sensors, risking hyperglycemia or diabetic ketoacidosis.
MedtronicMay 27, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Medtronic recalls MiniMed 720G insulin pumps (MMT-1809-1867) due to potential insulin over/under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
MedtronicFeb 13, 2026 - Lower riskMedical device
Medtronic MiniMed, Inc. recalls MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Medtronic MiniMed is a leading manufacturer of insulin pumps and diabetes management solutions. Their products help patients with diabetes manage their condition effectively.
Medtronic MiniMedJan 30, 2026 - Lower riskMedical device
Medtronic MiniMed, Inc. recalls InPen App, Model/CFN Number: MMT-8061 (Android Users)
Medtronic recalls InPen App version 7.5.0-8.0.0 for Android users. Uninstalling and reinstalling resets notification permissions, risking missed insulin alerts and hyperglycemia.
Medtr: a short, human brand name for headings (e.g. "Trsmima")Nov 13, 2025 - Stop using nowMedical device
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump
Medtronic recalls specific MiniMed 780G insulin pumps due to software errors that may suspend insulin delivery. Check your model and serial number.
Medtronic MiniMedNov 2, 2025 - Lower riskMedical device
Medtronic MiniMed, Inc. recalls CareLink Clinic, REF: MMT-7350
Medtronic recalls CareLink Clinic REF: MMT-7350 due to software error causing incorrect glucose data displays, which could lead to unsafe blood sugar levels. Affected users should check their device software version.
MedtronicOct 21, 2025 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)
Medtronic MiniMed recalls InPen App for iOS and Android users with software versions 7.0.0-7.5.0 due to missed insulin dose reminders. This could lead to hyperglycemia if users don't receive alerts for high glucose levels. The device itself still works for insulin delivery and CGM data.
Medtronic MiniMedJun 16, 2025 - Lower riskMedical device
Medtronic MiniMed, Inc. recalls Medtronic, Simplera Sensor, REF: MMT-5100JD1
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.
MedtronicMay 7, 2025 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
Medtronic MiniMed recalls specific InPen smart insulin pens due to potential incorrect assembly causing insulin cartridge issues. Affected units may lead to temporary hyperglycemia without backup insulin.
Medtronic MiniMedMar 4, 2025 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Medtronic MiniMed insulin pumps (770G models) may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or hyperglycemia. Affected units include MMT-1880 to MMT-1892 series.
Medtronic MiniMedJan 31, 2025 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 620G Insulin Pump, REF: MMT-1510, MMT-1710, MMT-1750; MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714,
Medtronic recalls certain MiniMed insulin pumps that may experience reduced battery life and shortened low battery alerts after being dropped or bumped, potentially causing unexpected shutdowns and insulin delivery interruptions.
MedtronicJul 31, 2024 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,
Medtronic recalls Guardian 4 Glucose Sensors with specific model numbers and lot codes due to potential glucose value errors that could cause hyperglycemia or hypoglycemia.
MedtronicNov 15, 2023
Medtronic MiniMed, Inc. recall questions
How many recalls has Medtronic MiniMed, Inc. had?
43 recalls from Medtronic MiniMed, Inc. are on record with U.S. safety agencies, from 2023–2026.
What is the most recent Medtronic MiniMed, Inc. recall?
Medtronic MiniMed, Inc. recalls Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product, dated Aug 20, 2026. Every Medtronic MiniMed, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Medtronic MiniMed, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medtronic MiniMed, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.