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

Baxter Healthcare Corporation 2022-03-30 Health serious FDA
Health · FDA · Recall #FDA-Z-0821-2022

Compella Therapy Air Supply Unit Recall

Issued March 30, 2022 · Baxter Healthcare Corporation

In March 2022, Baxter Healthcare Corporation recalled the Compella Therapy Air Supply Unit, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.

What you should do

  1. 1 Stop using Compella Therapy Air Supply Unit right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Baxter Healthcare Corporation 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
Baxter Healthcare Corporation
Category
Health
Recall date
March 30, 2022
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahamas, Bahrain, Belgium, Bermuda, Brazil, Cameroon, Canada
Recall number
FDA-Z-0821-2022
Made in
United States
Issuing agency
FDA

In context

  • Baxter Healthcare Corporation has 36 recalls in our database, including 5 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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