CARDINAL HEALTH CHAAX3000ARecalls & reported problems

Cardinal Health 200, LLC · HMEF Filter and Elbow With Gas Sampling Port · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 3
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885380057731), received between Aug 29, 2026 and Aug 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Connection Problem” (3 reports).

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.

Reports received per month

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

Most reported problems

Device problems

Connection Problem3

Patient problems

Insufficient Information3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

MalfunctionAug 29, 2026Connection Problem
Patient problems: Insufficient Information
MAUDE report 50510228 ↗
MalfunctionAug 29, 2026Connection Problem
Patient problems: Insufficient Information
MAUDE report 50510175 ↗
MalfunctionAug 29, 2026Connection Problem
Patient problems: Insufficient Information
MAUDE report 50510100 ↗

Device details

UDI-DI	`10885380057731`
Brand	CARDINAL HEALTH
Model	CHAAX3000A
Company	Cardinal Health 200, LLC
Product code	CAH · Filter, bacterial, breathing-circuit
Class	Class 2
FDA submission	K922492
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	Sep 22, 2020

Device type (GMDN): Microbial medical gas filter, single-use

A screening device intended to remove microbes from medical gases to prevent patient exposure during respiration, anaesthesia and/or endoscopy; it has no additional non-filtering functions. It is a small plastic housing containing a filter which will typically also filter other particulates (e.g., scale). This is a single-use device.

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All Filter, bacterial, breathing-circuit 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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