PlainRecalls
FDA Devices Moderate Class II Terminated

ambIT Cassette Filter Male Luer, Product Code: 220266

Reported: June 14, 2023 Initiated: April 24, 2023 #Z-1688-2023

Product Description

ambIT Cassette Filter Male Luer, Product Code: 220266

Reason for Recall

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

Details

Recalling Firm
Avanos Medical, Inc.
Units Affected
1155 total, 280 individually packaged
Distribution
Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.
Location
Alpharetta, GA

Frequently Asked Questions

What product was recalled?
ambIT Cassette Filter Male Luer, Product Code: 220266. Recalled by Avanos Medical, Inc.. Units affected: 1155 total, 280 individually packaged.
Why was this product recalled?
Some of the ambIT kits were potentially distributed without an air in-line filter.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 14, 2023. Severity: Moderate. Recall number: Z-1688-2023.