Avanos Medical, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1687-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 24, 2023

Date Posted: June 14, 2023

Recall Number: Z-1687-2023

Event ID: 92279

Reason for Recall:

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

Status: Terminated

Product Quantity: 40 cases (200 cassettes)

Code Information:

Lot Number (Expiration Date): 30191805 (17 Jan 2025)

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.

Voluntary or Mandated:

Voluntary: Firm initiated