Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due to Some of the ambIT kits were potentially distributed...

Date: April 24, 2023
Company: Avanos Medical, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Avanos Medical, Inc. directly.

Affected Products

SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568

Quantity: 40 cases (200 cassettes)

Why Was This Recalled?

Some of the ambIT kits were potentially distributed without an air in-line filter.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Avanos Medical, Inc.

Avanos Medical, Inc. has 37 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report