Medline DYNJAAHME30Recalls & reported problems

Medline Industries, Inc. · HME, TRACH · Class 1

Data updated Oct 16, 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 10888277333420), received between Sep 9, 2026 and Sep 9, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.

Reports received per month

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

Most reported problems

Device problems

Detachment of Device or Device Component1

Patient problems

Cough1

Recent adverse event reports

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

MalfunctionSep 9, 2026Detachment of Device or Device Component
It was reported that "THE TRACHS ARE FALLING APART AND THE FILTER FALL OUT WITHIN AN HOUR OF PUTTING IT ON.".
Patient problems: Cough
MAUDE report 50694876 ↗

Device details

UDI-DI	`10888277333420`
Brand	Medline
Model	DYNJAAHME30
Company	Medline Industries, Inc.
Product code	BYD · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 21, 2022

Device type (GMDN): Heat/moisture exchanger, single-use

A one-piece, canister-like device that connects in-line with a patient's artificial airway [e.g., an endotracheal (ET) tube], to capture the patient's exhaled heat and moisture so that they can be used to heat and humidify therapeutic gases inspired by the patient; it does not include a microbial filter. Commonly known as a heat & moisture exchanger (HME) or an "artificial nose", it is used when the patient is subjected to extended periods of breathing dry gases such as during anaesthesia or intensive care ventilation. This is a single-use device.

Other CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) devices

HUDSON RCI IPN042780
Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
1 recall3 reports
HUDSON RCI IPN042781
Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
1 recall1 report
DAR 353S19046
Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
1 recall1 report
DAR 354/5876
Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
25 reports
AVANOS 93816
Avanos Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
24 reports
HUDSON RCI IPN040673
Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
11 reports
Portex 450952-NL
Icu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
8 reports
Portex C45031682D-NL
Icu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)
8 reports

All CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) devices →

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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page