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Serious recall: Injury is possible or has been reported. Take action promptly.

Avanos Medical, Inc. 2023-06-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1684-2023

AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509 Recall

Issued June 14, 2023 · Avanos Medical, Inc.

In June 2023, Avanos Medical, Inc. recalled the AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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

What you should do

  1. 1 Stop using AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509 right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Avanos Medical, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Avanos Medical, Inc.
Category
Health
Recall date
June 14, 2023
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.
Recall number
FDA-Z-1684-2023
Made in
United States
Issuing agency
FDA

In context

  • Avanos Medical, Inc. has 5 recalls in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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