FDA Device recall Z-1031-2015
HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis
- FDA Device
- Class II
- terminated
- Published 2015-02-04
On 2015-02-04 the FDA classified a Class II recall of HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis by Baxter Healthcare, citing the keypad buttons on HomeChoice devices may be activated without the operator pressing them.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1031-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-21 |
| Published | 2015-02-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | 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 |
Product
HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis. Product codes 5C8310, 5C8310R, R5C8320, and 5C4474.
Reason
The keypad buttons on HomeChoice devices may be activated without the operator pressing them.
Identifiers
| code_info | all codes distributed between 4/15/2014 and 6/11/2014 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1031-2015%22
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