Z-0850-2019 Class II Terminated

Recalled by Baxter Healthcare Corporation — Deerfield, IL

Recall Details

Product Type
Devices
Report Date
February 27, 2019
Initiation Date
December 11, 2018
Termination Date
February 12, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,085 devices

Product Description

Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.

Reason for Recall

Potential for the software on Automated PD System cyclers which can cause shortened dwell times during a Cycle-Based therapy

Distribution Pattern

Worldwide Distribution - US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Distributed internationally to Canada and Japan.

Code Information

Product code T5C8500. All serial numbers are affected.