Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set Recalled by Baxter Healthcare Corporation Due to There is to an increase in complaints related...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set, REF 5C5479
Quantity: 339,936 devices
Why Was This Recalled?
There is to an increase in complaints related to failure alarms for Wet Cassette Integrity Test occurring on the Amia devices.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report