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t:slim Cartridge, t:lock, 10 Pack 1000991Recalls & reported problems

Tandem Diabetes Care, Inc. · t:slim Cartridge, t:lock, 10 Pack · Class 2

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 00853052007776), received between Oct 21, 2022 and Oct 21, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Physical Resistance/Sticking1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionOct 21, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT RESISTANCE WAS EXPERIENCED WHEN FILLING THE CARTRIDGE WITH INSULIN. THE ISSUE WAS RESOLVED BY PERFORMING A SUPPLY CHANGE. THERE WAS NO REPORTED ADVERSE IMPACT TO THE CUSTOMER¿S BLOOD GLUCOSE LEVEL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15651910 ↗

Other Pump, Infusion, Insulin devices

All Pump, Infusion, Insulin devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.