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Bardia® Universal Catheter Insertion Tray 802015Recalls & reported problems

C. R. Bard, Inc. · Bardia Universal Catheter Insertion Tray, 10 cc · 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 00801741051159), received between Feb 15, 2021 and Feb 15, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Component Missing1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionFeb 15, 2021Component Missing; Component Missing

    IT WAS REPORTED THAT THE (B)(6) 10 CC TRAY HAD NO LUBRICANT. PER FOLLOW-UP ON 08FEB2021, THE CUSTOMER STATED THAT THE LUBRICANT WAS MISSING FROM THE BARD INSERTION KIT.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement

    MAUDE report 11326666 ↗

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

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Sources and updates

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