Avanos Medical, Inc. SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568
Brand
Avanos Medical, Inc.
Lot Codes / Batch Numbers
Lot Number (Expiration Date): 30191805 (17 Jan 2025)
Products Sold
Lot Number (Expiration Date): 30191805 (17 Jan 2025)
Avanos Medical, Inc. is recalling SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568 due to Some of the ambIT kits were potentially distributed without an air in-line filter.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some of the ambIT kits were potentially distributed without an air in-line filter.
Recommended Action
Per FDA guidance
Avanos Medical notified customers on 04/24/2023 via email. Customers were instructed to evaluate their inventory of products to determine if any of the impacted product codes were present in their facility. The letter provided information identifying the affected product. It was indicated to segregate and contact Avanos to coordinate return/destruction of impacted product. Additionally, customers were instructed to complete and return the Acknowledgement Form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026