Bard® Clean-Cath® Intermittent Catheter 420710Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741038723), received between Oct 10, 2018 and Oct 10, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

Recent adverse event reports

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

• MalfunctionOct 10, 2018Component Missing

  IT WAS REPORTED THAT DURING THE STOCK WRITE-OFF FOR THE DEMO PURPOSES, THE SALES AND MARKETING ASSISTANT FOUND THAT A PRODUCT WAS MISSING FROM THE PACKAGING. THERE WAS NO PATIENT CONTACT.

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

  MAUDE report 7951152 ↗