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Avanos Medical, Inc. recalls SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568
Recalled June 14, 2023 · FDA recall Z-1687-2023 · Avanos Medical
Hazard
Some of the ambIT kits were potentially distributed without an air in-line filter. · FDA Class II
Units
40 cases (200 cassettes)
Sold at
Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.
Description
Some of the ambIT kits were potentially distributed without an air in-line filter.
Product
SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568
Manufacturer(s)
Avanos Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →