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Bard® Add-A-Foley Tray 304400ARecalls & reported problems

C. R. Bard, Inc. · Bard® Add-A-Foley Tray · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741130960), received between Sep 30, 2021 and Sep 30, 2021 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Component Missing1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 30, 2021Component Missing; Component Missing

    IT WAS REPORTED THAT THE INFECTION CONTROL TRAY CONTAINS EVERYTHING BUT THE 16 FRENCH CATHETER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12556126 ↗

Other COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.