Bard® Urine Meter Foley Catheter Tray With Bardex® Lubricath® Foley Catheter 902918Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741024870), received between Aug 7, 2018 and Aug 8, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 8, 2018Deformation Due to Compressive Stress; Material Deformation; Deformation Due to Compressive Stress

  IT WAS REPORTED THAT THE DRAIN BAG TUBING WAS KINKING, THEREFORE THE TUBING HAD TO MANIPULATED FOR URINE TO DRAIN.

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

  MAUDE report 7763817 ↗
• MalfunctionAug 7, 2018Restricted Flow rate; No Flow; Restricted Flow rate

  IT WAS REPORTED THAT THE DRAIN BAG WAS VAPOR LOCKED. ALLEGEDLY, THE URINE WOULD NOT DRAIN INTO THE BAG, THEREFORE IT WAS REPLACED.

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

  MAUDE report 7757621 ↗