HomeChoice/HomeChoice Pro Automated Personal Cycler — Class II medical device recall Z-1031-2015
Terminated recall by Baxter Healthcare Corp., reported 2015-02-04, distributed in AL, AR, AZ, CA, CO, CT, DC, FL…. The keypad buttons on HomeChoice devices may be activated without the operator pressing them.
| Recall number | Z-1031-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp., Deerfield, IL, United States |
| Recall initiated | 2014-10-21 |
| Classified | 2015-01-29 |
| Reported by FDA | 2015-02-04 |
| Terminated | 2015-09-01 |
| Distributed | AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MO, NC, NE, NJ, NM, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA, VT, WA, WI |
| Quantity | 200 |
Product
HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis. Product codes 5C8310, 5C8310R, R5C8320, and 5C4474.
Reason for recall
The keypad buttons on HomeChoice devices may be activated without the operator pressing them.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1031-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.