MiniLink® MMT-7725NARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169650817), received between Jul 6, 2016 and Jul 6, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Alarm System” (1 report).

2 other recalls cover devices cleared under the same FDA submission (P120010); they may or may not involve this specific model.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 6, 2016Device Alarm System; Failure to Sense; Incorrect Or Inadequate Test Results

  THE ISSUES I'VE BEEN HAVING ACTUALLY STARTED ABOUT A WEEK AGO NOW. I RECENTLY STARTED REUSING A MEDTRONIC INSULIN PUMP. I'M USING THE 530G WITH ENLITE CONTINUOUS GLUCOSE MONITORING SENSOR. I RECEIVED THE PUMP AND SENSOR BACK IN MARCH OF THIS YEAR (2016) AND BEGAN USING THEM IN (B)(6). ACCORDING TO MEDTRONIC, THEIR SENSOR HAS AN ACCURACY RANGE OF 20 PERCENT, MEANING THAT MY ACTUAL BLOOD GLUCOSE RANGE AND THE SENSOR GLUCOSE RANGE SHOULD BE WITHIN 20 PERCENT OF EACH OTHER. I AM HAVING MULTIPLE PROBLEMS WHERE THIS IS NOT THE CASE. MULTIPLE TIMES HAVE OCCURRED WHERE MY SENSOR GLUCOSE IS BETWEEN THE 70'S AND 50'S AND MY ACTUAL BLOOD GLUCOSE IS BETWEEN THE 150S AND 130S, OR VICE VERSA WHERE MY SENSOR GLUCOSE SAYS MY BLOOD SUGAR IS IN THE HIGH 200'S AND MY ACTUAL BLOOD GLUCOSE IS IN THE MID TO LOW 100S. EVERY TIME I HAVE CALLED MEDTRONIC TO REPORT AND SOLVE MY ISSUE, THEY HAVE NOT BEEN HELPFUL. WE WALK THROUGH TROUBLESHOOTING AND NOTHING GETS SOLVED AND IN A NUTSHELL I GET TOLD, "I'M SORRY THIS IS HAPPENING, THERE DOESN'T SEEM TO BE ANYTHING ELSE WE CAN DO TO HELP YOU." I AM ALSO GETTING CONSTANT WEAK SIGNALS BETWEEN THE INSULIN PUMP AND SENSOR TRANSMITTER. THEY ARE SUPPOSED TO TRANSMIT BE

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 5781714 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P120010. One submission often covers many models, so check the product and lot details in each record.

• Z-1751-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 530G Insulin Pump (MMT-551, MMT-751)
• Z-2544-2014 · Mar 13, 2014 · Terminated
  Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K