Medline DYNCSTP14TRecalls & reported problems

Medline Industries, Inc. · CATH,CLOSED SUCTION,14FR,T-PC,TRACH,24HR · Class 1

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884389145982), received between Aug 22, 2024 and Aug 22, 2024 — classified as 1 injury.

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

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Appropriate Device Problem Term/Code Not Available1

Patient problems

Hypoxia1

Recent adverse event reports

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

InjuryAug 22, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE PATIENT WAS "DETERIORATING MEDICALLY" AND "EXPERIENCED HYPOXIA" DUE TO THE CLOSED SUCTION "CONTINUALLY SUCTIONING AS IF THE THUMB VALVE WAS ENGAGED".
Patient problems: Hypoxia
MAUDE report 20033759 ↗

Device details

UDI-DI	`10884389145982`
Brand	Medline
Model	DYNCSTP14T
Company	Medline Industries, Inc.
Product code	BSY · CATHETERS, SUCTION, TRACHEOBRONCHIAL
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Nov 28, 2022

Device type (GMDN): Surgical suction system collection container, single-use

A sealable container (e.g., cylindrical, bottle-shaped, pouch) intended to be used as a component of a surgical suction system to collect aspirated materials (e.g., blood/bodily fluids, gases, body tissues, calculi) from a surgical site for disposal (e.g., to prevent backflow) or diagnostic/therapeutic purposes (e.g., tissue or polyp trap). It may be used singularly or connected in a series to provide greater capacity, and may be graduated to facilitate determination of the quantity of its contents; it may also be used in conjunction with aspiration liners and may include lid, microbial/hydrophobic filters or tubing. This is a single-use device.

Other CATHETERS, SUCTION, TRACHEOBRONCHIAL devices

Ballard* Closed Suction System 93826
Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall70 reports
Ballard* Closed Suction System 92431
Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
78 reports
Medline DYNCPDS14
Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall16 reports
Ballard* Turbo-Cleaning Closed Suction System 98965
Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall16 reports
Ballard* Turbo-Cleaning Closed Suction System 98263
Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall11 reports
Ballard* Closed Suction System for Adults 98310
Avanos Medical, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall1 death9 reports
Medline DYNCPTP14T
Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall6 reports
Medline DYNCPTP14
Medline Industries, Inc. · CATHETERS, SUCTION, TRACHEOBRONCHIAL
1 recall4 reports

All CATHETERS, SUCTION, TRACHEOBRONCHIAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.