Medtronic MiniMed, Inc. recalls Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) Software Version:…
A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier experienced failure of the long-acting dose reminder after updating…
Read the official notice →- Date
- 2026-10-28
- Country
- United States
- Brand
- Medtronic MiniMed
- Product
- Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) Software Version:…
- Classification
- Class II
- Units
- Worldwide - U.S. Nationwide distribution in the states of AL, CA, CT, FL, LA,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Medtronic MiniMed recalls
- 2026-10-28
Medtronic MiniMed, Inc. recalls CareLink Clinic, REF: MMT-7350
CareLink Clinic software version 4.4A includes a software defect in the Settings Calculator feature in which the calculation logic fails to use custom values entered by healthcare professionals (HCPs) for Total Daily…
- 2026-10-14
Medtronic MiniMed, Inc. recalls Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The…
Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed verification test results in one or more of 9 functional tests. The…
FDA · DeviceMedtronic MiniMed, Inc.U.S. Nationwide distribution in the states of AR, AZ, CO, FL, KS, KY, LA, MI,…Official notice →- 2026-08-26
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing…
FDA · DeviceMedtronic MiniMed, Inc.International distribution to the countries of Germany, Denmark, Austria,…Official notice →- 2026-07-29
Medtronic MiniMed, Inc. recalls MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This…
FDA · DeviceMedtronic MiniMed, Inc.Worldwide - US Nationwide distribution in the states and territories of PR,…Official notice →- 2026-07-15
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53…
FDA · DeviceMedtronic MiniMed, Inc.International distribution to the countries of Spain, Great Britain,…Official notice →- 2026-04-08
Medtronic MiniMed, Inc. recalls MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the…
FDA · DeviceMedtronic MiniMed, Inc.Worldwide - US Nationwide distribution including in the states of OR, CA, AZ,…Official notice →
USOther drugs & medical recalls in the United States
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FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.Official notice →Solstice Corporation recalls Xact mole marker for mammography Model/Catalog Number: M15RM
The radiopaque material may detach from the marker. In some cases, artifact was noted and attributed to the detached material.
FDA · DeviceSolstice CorporationWorldwide - US Nationwide distribution in the states and territory of CA, FL,…Official notice →Medtronic Neuromodulation recalls InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030
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Implants were found in the field with orange sterilzation indicators which means implants were not exposed to sterilization.
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