Compella Therapy Air Supply Unit recall
Compella Therapy Air Supply Unit
Why was Compella Therapy Air Supply Unit recalled?
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 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?
All lots/serial numbers UDI information: Compella Therapy Air Supply Unit - 00887761013803
- Product
- Compella Therapy Air Supply Unit
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 6022 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahamas, Bahrain, Belgium, Bermuda, Brazil, Cameroon, Canada, Estonia, Finland, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Jamaica, Jordan, Kuwait, Mexico, Netherlands, New Zealand, Norway, Oman, Poland, Qatar, Romania, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkmenistan, UAE, and UK.
- Recall date
- March 30, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)