Bard® Foley Tray with Hydrophilic-Coated Foley Catheter 861414Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741024757), received between Jan 29, 2019 and Jan 29, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inaccurate Flow Rate” (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.

• MalfunctionJan 29, 2019Inaccurate Flow Rate; No Flow; Inaccurate Flow Rate

  IT WAS REPORTED THAT THE FOLEY CATHETERS WERE NOT DRAINING. ADDITIONAL INFORMATION WAS RECEIVED ON 10 JAN 2019 THAT URINE BACKED UP IN THE TUBING AND WOULD NOT DRAIN UNTIL THE PATIENT WAS PLACED IN A STANDING POSITION. NO MEDICAL INTERVENTION WAS REPORTED.

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

  MAUDE report 8285961 ↗