TANDEM 71363052Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010481658), received between Sep 4, 2020 and Dec 21, 2021 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 21, 2021Break; Break

  IT WAS REPORTED THAT AFTER THR THE MDR NOTICES THAT THE TANDEM TRL SHELL 52MM WAS CHIPPED. AS THIS WAS NOTICED AFTER PROCEDURE, NO CASE WAS INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13054602 ↗
• MalfunctionMar 8, 2021Break; Break

  IT WAS REPORTED THAT, AFTER SURGERY IT WAS NOTICED THAT THE INSIDE RING OF THE TANDEM TRIAL SHELL HEADS ((B)(4)) ARE BROKEN AND CANNOT BE PROPERLY CLEANED. INCIDENT OCCURRED AFTER THE PROCEDURE; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11431659 ↗
• MalfunctionSep 4, 2020Defective Device; Defective Device

  IT WAS REPORTED THAT DURING INSPECTION THE TANDEM TRL SHELL'S WERE FOUND WITHOUT THREADS. THESE ARE OLD STYLES THAT NEVER HAD THREADS. NO CASE RELATED, THEREFORE, NO PATIENT INVOLVED.

  Patient problems: No Patient Involvement

  MAUDE report 10497170 ↗