Magic3™ Intermittent Catheter 53916Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741068706), received between Dec 5, 2018 and Apr 10, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Damaged Prior to Use” (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.

• MalfunctionApr 10, 2019Difficult to Insert

  IT WAS REPORTED THAT THE MAGIC 3 INTERMITTENT CATHETER WAS DIFFICULT TO INSERT INTO THE BLADDER DUE TO BLOOD CLOTS THAT FORMED IN THE BLADDER AS A RESULT OF RADIATION TREATMENTS. THE PATIENT EXCHANGED THE PRODUCT FOR A PRODUCT BETTER SUITED TO HIS CONDITION. NO MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 8501101 ↗
• MalfunctionDec 5, 2018Device Damaged Prior to Use; Device Damaged Prior to Use; Material Deformation

  IT WAS REPORTED THAT THE ANTIBACTERIAL COATING ON THE MAGIC 3 CATHETER WAS VERY ROUGH AND FELT LIKE "SAND PAPER" EVEN WITH THE LUBRICANT. NO PATIENT IMPACT WAS REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8133432 ↗