Medline DYNCPTP14Recalls & reported problems
Medline Industries, Inc. · CLEARPRO,CLOSED SXN,14FR,T-PC,ETT · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888277703469), received between Aug 14, 2025 and Aug 31, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Aug 3, 2022Open, Classified
Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the patient suctioning process.
Z-1857-2022 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
- Fluid/Blood Leak1
- Gas/Air Leak1
- Loose or Intermittent Connection1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Respiratory Insufficiency1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 31, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50531467 ↗MalfunctionAug 28, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50502639 ↗MalfunctionMay 1, 2026Loose or Intermittent Connection
PER REPORT, " THE SUCTION CATHETER CAME A PART WHILE BEING ATTACHED TO THE PATIENT FOR LESS THAN 12 HOURS."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25061037 ↗InjuryAug 14, 2025Break; Material Separation; Gas/Air Leak; Break; Material Separation; Gas/Air Leak
ACCORDING TO THE CUSTOMER, THE SUCTION CATHETERS HAVE BEEN "BREAKING", "LEAKING", SEPARATING AT THE HINGED ELBOW, THE GREEN BAND COMES OFF AROUND THE SLEEVE, AND THEY ARE "FLIMSY" CAUSING DIFFICULTY WHEN SUCTIONING THICK SECRETIONS.
Patient problems: Respiratory Insufficiency
MAUDE report 22804621 ↗
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
- Medline DYNCPDS14Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall16 reports
- Ballard* Turbo-Cleaning Closed Suction System 98965Avanos Medical, 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 DYNCPDS14TMedline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL1 recall3 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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