FDAClass IIJune 14, 2023

ambIT Cassette Filter Male Luer recall

ambIT Cassette Filter Male Luer, Product Code: 220266

Why was ambIT Cassette Filter Male Luer recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Number (Expiration Date): F201701 (17 Jan 2025)

Product
ambIT Cassette Filter Male Luer, Product Code: 220266
Recalling firm
Avanos Medical, Inc.
Quantity
1155 total, 280 individually packaged
Distribution
Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.
Recall date
June 14, 2023
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls