Glooko Mobile Insulin Dosing System (MIDS) Android & iOS Mobile Application 5.xRecalls & reported problems
Glooko, Inc. · Glooko Mobile Insulin Dosing System (MIDS) is an insulin dose calculator. The Glooko MIDS Mobile Application is only available to patients who have been prescribed MIDS by their heath care provider. The mobile application can be downloaded by patients from the Google Play Store for Android and from the Apple App Store for iOS operating systems. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00855093008002), received between Aug 10, 2018 and Aug 10, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Computer Software Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Computer Software Problem1
- Failure to Transmit Record1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 10, 2018Computer Software Problem; Failure to Transmit Record
A USER REPORTED THAT RECENT BLOOD GLUCOSE READINGS FROM THEIR BAYER CONTOUR NEXT ONE METER WERE NOT BEING TRANSFERRED TO THE GLOOKO MOBILE APPLICATION. AS A RESULT, THE USER WAS NOT ABLE TO ACCESS THE NEW BLOOD GLUCOSE READINGS ON THE GLOOKO APPLICATION. NO ADVERSE EVENT WAS REPORTED. GLOOKO ENGINEERING INVESTIGATED THE ISSUE AND WAS ABLE TO REPRODUCE IT IN-HOUSE, AND NOTED THAT THE ISSUE WAS ONLY SEEN WITH READINGS FROM BAYER CONTOUR NEXT ONE METERS. A SOFTWARE UPDATE WAS IMPLEMENTED TO ADDRESS THE SYNCING ISSUE WITH BAYER CONTOUR NEXT ONE METERS AND THE INVESTIGATION WAS CLOSED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7774755 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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