Bard® Urine Meter Foley Catheter Tray With Bard® Hydrophilic-Coated Foley 800366Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741020131), received between Nov 20, 2020 and Nov 20, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Deflation Problem” (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.

• InjuryNov 20, 2020Deflation Problem; Deflation Problem

  IT WAS REPORTED THAT THE CATHETER'S BALLOON WAS UNABLE TO ASPIRATE WITH SYRINGE. INJECTED BALLOON PORT WITH 5CC STERILE WATER AND DID NOT ASPIRATE BACK. THEN BALLOON PORT WAS CUT AND DID NOT DRAIN AND 4.025 WIRE ADVANCED LENGTH OF FOLEY AND HELD IN PLACE, WATER FROM BALLOON PORT DRAINED AROUND WIRE THEN THE CATHETER REMOVED EASILY.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; No Code Available; No Consequences Or Impact To Patient; Pain

  MAUDE report 10877183 ↗