Bard® Clean-Cath® Intermittent Catheter 423712Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741038860), received between Jul 17, 2017 and Apr 4, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionApr 4, 2022Nonstandard Device; Nonstandard Device

  IT WAS REPORTED THAT THE INTERMITTENT CATHETER WAS NOT CURVED ENOUGH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13995025 ↗
• MalfunctionApr 8, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT THE CATHETER WAS TWISTED AND UNABLE TO USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11636937 ↗
• MalfunctionAug 7, 2020Loose or Intermittent Connection; Material Twisted/Bent

  IT WAS REPORTED THAT THE PATIENT STATED THERE WAS SOME LOOSE CATHETERS THAT WERE THROWN IN THE BOX WHICH THEY WERE TWISTED AND BENT. ALSO STATED THESE WERE NOT SOFT CATHETERS.

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

  MAUDE report 10382192 ↗
• MalfunctionJul 17, 2017Scratched Material

  IT WAS REPORTED THAT THE CATHETER HAD A SHARP TIP.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6720256 ↗