Magic3™ Intermittent Catheter 51314Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00801741068133), received between Nov 20, 2018 and Mar 16, 2022 — classified as 4 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (4 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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 16, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE MAGIC 3 INTERMITTENT CATHETERS WERE HARD TO INSERT AND DID NOT WORK FOR THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13777527 ↗
• InjuryMar 25, 2020Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE CATHETERS WERE CAUSING THE PATIENT UTIS.

  Patient problems: Urinary Tract Infection

  MAUDE report 9878145 ↗
• InjuryJan 13, 2020Patient-Device Incompatibility; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED A UTI WITH USE OF THE CATHETER. IT WAS UNKNOWN WHAT MEDICAL INTERVENTIONS WERE GIVEN FOR THE UTI.

  Patient problems: Urinary Tract Infection

  MAUDE report 9582946 ↗
• InjuryAug 5, 2019Patient-Device Incompatibility; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE PATIENT DEVELOPED A URINARY TRACT INFECTION WHILE USING THE MAGIC 3 CATHETER; TREATMENT PROVIDED IS UNKNOWN.

  Patient problems: Urinary Tract Infection

  MAUDE report 8861823 ↗
• InjuryMay 3, 2019Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE PATIENT DEVELOPED A KIDNEY INFECTION ALLEGEDLY FROM USING THE CATHETERS. THE PATIENT NO LONGER USED CATHETERS PER THE DOCTOR'S INSTRUCTIONS.

  Patient problems: Unspecified Infection

  MAUDE report 8579104 ↗
• MalfunctionFeb 21, 2019Misassembled; Manufacturing, Packaging or Shipping Problem; Misassembled

  IT WAS REPORTED THAT THE EYELETS ON THE CATHETERS WERE NOT PUNCHED THROUGH FULLY, WHICH MADE THEM UNUSABLE. NO MEDICAL INTERVENTION WAS REQUIRED.

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

  MAUDE report 8359220 ↗
• MalfunctionNov 20, 2018Device Damaged Prior to Use; Material Too Rigid or Stiff; Device Damaged Prior to Use

  IT WAS REPORTED THAT THE CATHETERS WERE VERY ROUGH ON THE END.

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

  MAUDE report 8091238 ↗