Magic3™ Intermittent Catheter 51914Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741068294), received between Sep 5, 2018 and Mar 15, 2019 — classified as 1 injury, 1 malfunction.

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.

• InjuryMar 15, 2019Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN URINARY TRACT INFECTION AFTER USING THE MAGIC 3 CATHETER. THE PATIENT WAS TREATED WITH ANTIBIOTICS. SHE HAD DECIDED TO RESUME USING THE CURE CATHETER.

  Patient problems: Urinary Tract Infection

  MAUDE report 8424092 ↗
• MalfunctionSep 5, 2018Device Damaged Prior to Use; Material Integrity Problem; Device Damaged Prior to Use

  IT WAS REPORTED THAT PATIENT NOTICED SHARP EDGES UPON REMOVING THE CATHETER. THE PATIENT DID EXPERIENCE SELF-LIMITED BLEEDING; HOWEVER; THERE WAS NO MEDICAL INTERVENTION REQUIRED.

  Patient problems: Hemorrhage/Blood Loss/Bleeding; Patient Problem/Medical Problem

  MAUDE report 7846176 ↗