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Catheter and Glove Suction Kit 0140040Recalls & reported problems

C. R. Bard, Inc. · Catheter and Glove Suction Kit with Solution Container, CSR Wrap and Two Vinyl Gloves · Class 1

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 00801741050633), received between Dec 5, 2018 and Dec 5, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Nonstandard Device” (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

  • Nonstandard Device1
  • Suction Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1
  • 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.

  • MalfunctionDec 5, 2018Nonstandard Device; Nonstandard Device; Suction Problem

    IT WAS REPORTED THAT THE CATHETER FROM THE PLASTIC SUCTION CATHETER KIT HAD UNSPECIFIED VISUAL DEFECTS. THE PRODUCT WAS DETAINED AT THE BORDER BY FDA CUSTOMS WHERE IT WAS RANDOMLY SELECTED TO BE SAMPLED AND SENT TO AN FDA SELECTED LABORATORY FOR INSPECTION.

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

    MAUDE report 8134893 ↗

Other CATHETERS, SUCTION, TRACHEOBRONCHIAL devices

All CATHETERS, SUCTION, TRACHEOBRONCHIAL devices →

Sources and updates

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