Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HomeChoice/HomeChoice Pro Automated Personal Cycler Recalled by Baxter Healthcare Corp. Due to The keypad buttons on HomeChoice devices may be...
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 Corp. directly.
Affected Products
HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis. Product codes 5C8310, 5C8310R, R5C8320, and 5C4474.
Quantity: 200
Why Was This Recalled?
The keypad buttons on HomeChoice devices may be activated without the operator pressing them.
Where Was This Sold?
This product was distributed to 35 states: AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, LA, MD, MA, MI, MO, NE, NV, NJ, NM, NY, NC, OH, OK, PA, SC, TN, TX, UT, VT, VA, WA, WI
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report