Health product recall

Prismax Control Unit

Last updated

Summary

Product
Prismax Control Unit
Issue
Medical devices - Inaccurate test or measurement results
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or Serial Number

Model or catalog number

Prismax Control Unit

All lots.

955558, 955725

Issue

Baxter Corporation is issuing a correction for the Prismax. If the operator initiates therapy by entering a value other than the default value for the patient gain/loss limit or the return pressure drop limit and uses the same patient function, the Prismax system will return the patient gain/loss limit or the return pressure drop limit to the default value, rather than the non-default value entered at the initiation of treatment.

Recall start date: Mar 17, 2022

Additional information

Details
Original published date: 2022-03-31
Alert / recall type
Health product recall
Category
Health product - Medical device - Gastroenterology & Urology
Companies

Baxter Healthcare Sa

Po Box 8010, Zurich

Switzerland, 8010

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-64030