Baxter Healthcare Corp.: Medical Device Recall in 2015 - (Recall #: Z-1031-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis. Product codes 5C8310, 5C8310R, R5C8320, and 5C4474.

Product Classification:

Class II

Date Initiated: October 21, 2014

Date Posted: February 4, 2015

Recall Number: Z-1031-2015

Event ID: 70232

Reason for Recall:

The keypad buttons on HomeChoice devices may be activated without the operator pressing them.

Status: Terminated

Product Quantity: 200

Code Information:

all codes distributed between 4/15/2014 and 6/11/2014

Distribution Pattern:

AL, AR, AZ, CA, CO, CT, 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 and District of Columbia

Voluntary or Mandated:

Voluntary: Firm initiated