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Bard® Add-A-Foley Tray 896300Recalls & reported problems

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

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00801741029264), received between Aug 8, 2017 and Aug 8, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

Device problems

  • Device Contamination with Chemical or Other Material1
  • Improper or Incorrect Procedure or Method1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionAug 8, 2017Improper or Incorrect Procedure or Method; Device Contamination with Chemical or Other Material

    IT WAS REPORTED THAT THERE WERE BLACK SPOTS ON THE INSIDE OF THE DRAIN BAG NEAR THE AIR VENT. THE DRAIN BAG WAS ALLEGEDLY POSITIONED FLAT ON THE FLOOR AND WAS NOT ALLOWED TO BECOME FULL. THE DRAIN BAG WAS USED WITH A SILVER COATED CATHETER. NO PATIENT INJURY WAS REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6776013 ↗

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

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Sources and updates

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