Magic3 Touchless™ Hydrophilic Intermittent Catheter System 58714Recalls & reported problems
C. R. Bard, Inc. · Magic3 Touchless™ Hydrophilic Intermittent Catheter System · Class 2
Data updated Oct 18, 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 00801741103988), received between Nov 8, 2017 and Nov 8, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 18, 2026.
Most reported problems
Device problems
- Device Operates Differently Than Expected1
- Difficult to Insert1
- Product Quality Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 8, 2017Difficult to Insert; Product Quality Problem; Device Operates Differently Than Expected; Product Quality Problem
IT WAS REPORTED THAT AFTER BURSTING THE WATER PACKET AND LUBRICATING THE CATHETER, THE DEVICE LACKED LUBRICITY AND WAS UNABLE TO BE FULLY INSERTED. THE NURSE REPORTED THAT THE CATHETER ONLY RETURNED 100 ML OF URINE. THE CATHETER WAS REPORTEDLY REPLACED AND RETURNED 1200 ML OF URINE WITH THE REPLACED CATHETER. IT WAS ALSO REPORTED THAT THE PATIENT EXPERIENCED PAIN.
Patient problems: Pain
MAUDE report 7009276 ↗
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- Bardex® Lubri-Sil® I.C. All-Silicone Temp Sensing Foley Catheter 119316MC. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES231 reports
- Bardex® Lubri-Sil® I.C. Temperature-Sensing All-Silicone Foley Catheter 119316C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES198 reports
- Bardex® I.C. Foley Catheter 0165SI18C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES181 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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