Catheter and Glove Suction Kit 0140080Recalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741050671), received between Apr 9, 2018 and Dec 6, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Defective 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
- Defective Device1
- Device Operates Differently Than Expected1
- Inadequate Instructions for Healthcare Professional1
- Nonstandard Device1
Patient problems
- No Known Impact Or Consequence To Patient2
- No Patient Involvement2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2018Nonstandard Device; Nonstandard Device; Defective Device
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 8138277 ↗MalfunctionApr 9, 2018Inadequate Instructions for Healthcare Professional; Inadequate Instructions for Healthcare Professional; Device Operates Differently Than Expected
IT WAS REPORTED THAT THE SUCTION CATHETER WAS THICKER THAN USUAL.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 7407370 ↗
Other CATHETERS, SUCTION, TRACHEOBRONCHIAL devices
- Ballard* Closed Suction System 93826Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall70 reports
- Ballard* Closed Suction System 92431Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL78 reports
- Ballard* Turbo-Cleaning Closed Suction System 98965Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall16 reports
- Medline DYNCPDS14Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall16 reports
- Ballard* Turbo-Cleaning Closed Suction System 98263Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall11 reports
- Ballard* Closed Suction System for Adults 98310Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall1 death9 reports
- Medline DYNCPTP14TMedline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall6 reports
- Medline DYNCPTP14Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall4 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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