Recall Atlas
Drugs & medicalClass II

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…

Read the official notice →
Date
2026-10-28
Country
United States
Brand
Medtronic MiniMed
Product
CareLink Clinic, REF: MMT-7350
Classification
Class II
Units
US Nationwide distribution in the state of KS.
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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

  1. 2026-10-28
  2. Drugs & medicalClass II

    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…

    FDA · DeviceMedtronic MiniMed, Inc.Worldwide - U.S. Nationwide distribution in the states of AL, CA, CT, FL, LA,…Official notice →
  3. 2026-10-14
  4. Drugs & medicalClass II

    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 →
  5. 2026-08-26
  6. Drugs & medicalClass II

    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 →
  7. 2026-07-29
  8. Drugs & medicalClass II

    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 →
  9. 2026-07-15
  10. Drugs & medicalClass II

    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 →
  11. 2026-04-08
  12. Drugs & medicalClass II

    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 →
All 21 Medtronic MiniMed recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-28
  2. Drugs & medicalClass II

    Life Technologies Holdings Pte Ltd recalls Ion Torrent Genexus Dx with software, Catalog: A40003539, which supports the Ion Torrent Genexus Dx Integrated Sequencer

    DNA or RNA sequencing system software has vulnerabilities.

    FDA · DeviceLife Technologies Holdings Pte LtdUS Nationwide distribution in the states of PA, NC, CO, CA, LA, KY, NY, AZ,…Official notice →
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    FDA · DeviceTECHNO-PATH MANUFACTURING LTD.US Nationwide distribution in the state of Massachusetts.Official notice →
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    Beckman Coulter, Inc. recalls ROTOR ASSY-SW41, Reference Number 331362, when the rotors are installed in the following centrifuges: Optima XPN-100 (Model Numbers A99846…

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    FDA · DeviceBeckman Coulter, Inc.US Nationwide distribution.Official notice →
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    Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+) and falsely decreased calcium (Ca++) results which have the…

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