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Magic3™ Hydrophilic Intermittent Catheter, Female 51614SRecalls & reported problems

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

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 00801741072499), received between Feb 5, 2019 and May 11, 2020 — classified as 4 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1
  • Device Damaged Prior to Use1
  • Incorrect Measurement1
  • Nonstandard Device1
  • Product Quality Problem1
  • Scratched Material1

Patient problems

  • Abrasion1
  • No Code Available1
  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1
  • No Patient Involvement1
  • Pain1

Recent adverse event reports

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

  • MalfunctionMay 11, 2020Product Quality Problem; Product Quality Problem

    IT WAS REPORTED THAT THE CATHETERS LACKED LUBRICITY CAUSING PAINFUL INSERTION. NO MEDICAL INTERVENTION WAS REPORTED. IT IS UNKNOWN IF THE PATIENT WAS ABLE TO FULLY INSERT AND VOID.

    Patient problems: Pain

    MAUDE report 10043136 ↗
  • MalfunctionSep 18, 2019Incorrect Measurement; Incorrect Measurement

    IT WAS REPORTED THAT THE MAGIC 3 CATHETER WAS BIGGER THAN USUAL.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9081554 ↗
  • MalfunctionSep 16, 2019Device Damaged Prior to Use; Scratched Material; Device Damaged Prior to Use

    IT WAS REPORTED THAT THE SURFACE OF THE MAGIC 3 CATHETER WAS ROUGH, WHICH ALLEGEDLY CAUSED IT TO SCRATCH THE PATIENT DURING USE. NO MEDICAL INTERVENTION WAS REPORTED.

    Patient problems: Abrasion; No Code Available

    MAUDE report 9071123 ↗
  • MalfunctionFeb 5, 2019Nonstandard Device; Appropriate Device Problem Term/Code Not Available; Nonstandard Device

    IT WAS REPORTED THAT THE MAGIC 3 CATHETER FAILED THE VISUAL ANALYSIS EVALUATION. FDA CUSTOMS DETAINED THIS PRODUCT AT THE BORDER WHERE IT WAS RANDOMLY SELECTED TO BE SAMPLED AND SENT TO AN FDA SELECTED LABORATORY FOR INSPECTION.

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

    MAUDE report 8304703 ↗

Other Catheter care tray devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.