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Magic3™ Intermittent Catheter 53914Recalls & 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
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741068690), received between Nov 8, 2018 and Nov 8, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 8, 2018Difficult to Insert; Difficult to Insert

    IT WAS REPORTED THAT THE CATHETER WAS DIFFICULT TO INSERT AND THE PATIENT WAS UNABLE TO USE THE CATHETER.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8052551 ↗

Other CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES devices

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Sources and updates

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