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Magic3™ Intermittent Catheter 53912Recalls & reported problems

C. R. Bard, Inc. · Magic3™ Intermittent Catheter Antibacterial Coated Silicone, Male · Class 2

All models of Magic3 Intermittent Catheter (37)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741068683), received between Jun 9, 2017 and Jun 9, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (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

Device problems

  • Material Deformation1
  • Wrinkled1

Patient problems

  • No Known Impact Or Consequence To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 9, 2017Material Deformation

    IT WAS REPORTED THAT THE CATHETER TIP WAS "ROLLED UP".

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6632656 ↗
  • MalfunctionJun 9, 2017Wrinkled

    IT WAS REPORTED THAT THE TIP OF THE CATHETER WAS WRINKLED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6632059 ↗

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Sources and updates

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