Bard® Clean-Cath® Intermittent Catheter 420718Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741038761), received between Apr 3, 2018 and Apr 4, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Expiration Issue” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 4, 2018Device Expiration Issue; Improper or Incorrect Procedure or Method

  IT WAS REPORTED THAT THE PATIENT USED A CATHETER THAT EXPIRED IN 2017. PER ADDITIONAL INFORMATION RECEIVED, THE PRODUCT WAS ALREADY EXPIRED BEFORE BEING SHIPPED TO THE PATIENT.

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

  MAUDE report 7395605 ↗
• MalfunctionApr 3, 2018Device Expiration Issue

  IT WAS REPORTED THE PATIENT USED A CATHETER THAT EXPIRED IN 2017. PER ADDITIONAL INFORMATION, THE PRODUCT WAS ALREADY EXPIRED BEFORE IT WAS SHIPPED TO THE PATIENT.

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

  MAUDE report 7392935 ↗