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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
- Homechoice Automated PD System
- 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