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Magic3™ Intermittent Catheter 52308Recalls & reported problems

C. R. Bard, Inc. · Magic3™ Intermittent Catheter, Pediatric · Class 2

All models of Magic3 Intermittent Catheter (37)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741068348), received between Oct 26, 2017 and Jul 9, 2020 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Product Quality Problem” (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

Device problems

  • Product Quality Problem2
  • Fluid/Blood Leak1
  • Incorrect Measurement1
  • Insufficient Device Problem Information1
  • Leak/Splash1
  • Material Puncture/Hole1
  • Therapeutic or Diagnostic Output Failure1

Patient problems

  • No Consequences Or Impact To Patient2
  • No Known Impact Or Consequence To Patient2
  • Pain2
  • Blood Loss1
  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 9, 2020Therapeutic or Diagnostic Output Failure; Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT 2 OF THE MAGIC 3 CATHETERS WERE FAILED IN THE PATIENT.

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

    MAUDE report 10253320 ↗
  • MalfunctionJun 25, 2020Fluid/Blood Leak; Fluid/Blood Leak; Leak/Splash; Material Puncture/Hole

    IT WAS REPORTED THAT THE FOLEY CATHETER BEGAN TO LEAK URINE FROM THE BASE OF THE Y- SITE. THE FOLEY WAS REPLACED WITH ANOTHER 8FR BARD CATHETER AND NOTICED URINE LEAK FROM THE EXACT SAME SPOT. THE CUSTOMER ALSO STATED THAT BOTH THE CATHETERS HAD A HOLE IN THE SAME SPOT.

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

    MAUDE report 10194784 ↗
  • MalfunctionOct 26, 2017Incorrect Measurement; Product Quality Problem

    IT WAS REPORTED THAT THE CATHETER APPEARED TO BE THICKER THAN USUAL. THE PATIENT ALLEGEDLY EXPERIENCED PAIN AND SELF-LIMITED BLEEDING.

    Patient problems: Blood Loss; Pain

    MAUDE report 6979773 ↗
  • MalfunctionOct 26, 2017Product Quality Problem

    IT WAS REPORTED THAT THE CATHETER APPEARED TO BE THICKER THAN USUAL. THE PATIENT EXPERIENCED PAIN AND SELF-LIMITED BLEEDING.

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Pain

    MAUDE report 6979766 ↗

Other CATHETER, UROLOGICAL devices

All CATHETER, UROLOGICAL devices →

Sources and updates

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