Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Automated Peritoneal Dialysis System. Used for automatic control of dialysis Recalled by Baxter Healthcare Corporation Due to The electrical safety testing was not properly performed...
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
Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges.
Quantity: 16 units
Why Was This Recalled?
The electrical safety testing was not properly performed on the impacted devices and additional testing is required
Where Was This Sold?
This product was distributed to 10 states: AL, AZ, AR, FL, IL, NY, ND, OH, TX, WA
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