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Health product recall

Homechoice Automated and Homechoice Pro Automated PD Systems (2015-01-22)

Starting date:
January 22, 2015
Posting date:
January 30, 2015
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-43567

Recalled Products   

  1. Homechoice Automated PD System
  2. Homechoice Pro Automated PD System

Reason

Baxter Corporation is issuing a device correction for HOMECHOICE and HOMECHOICE PRO devices shipped without the English (language) patient at-home guide kit. Home peritoneal dialysis patients who received a device without the patient at-home guide kit are being contacted by telephone and will be immediately shipped the guide kit.

Affected products

A. Homechoice Automated PD System

Lot or serial number
  • 13294
  • 16324
  • 19527
  • 664038
  • 664626
Model or catalog number

5C4471R
 

Companies
Manufacturer
Baxter Healthcare Corporation
1 Baxter Parkway
Deerfield
60015
Illinois
UNITED STATES

B. Homechoice Pro Automated PD System

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

5C8310R

Companies
Manufacturer
Baxter Healthcare Corporation
1 Baxter Parkway
Deerfield
60015
Illinois
UNITED STATES