Magic3™ Intermittent Catheter 52306Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741068331), received between Oct 10, 2017 and Oct 13, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 13, 2017Incorrect Measurement

  IT WAS REPORTED THAT THE DIAMETER OF THE CATHETER APPEARED TO BE DIFFERENT SIZES CAUSING SOME AREAS OF THE CATHETER TO FEEL SOFT AND SOME HARD.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6948735 ↗
• MalfunctionOct 10, 2017Difficult to Insert; Material Integrity Problem

  IT WAS REPORTED THAT THE DIAMETER OF THE CATHETER WAS BIGGER THAN USUAL, AND THE CATHETER WAS DIFFICULT TO INSERT. THE DEVICE WAS STILL ABLE TO BE INSERTED AND USED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6938349 ↗