Product Wiki · Recalls · Health Canada — Medical Devices

PRISMAX CONTROL UNIT (2021-10-05) — recall 62934

Health Canada — Medical Devices · Canada · 2021-10-21 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
62934
Date of alert
2021-10-21
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Baxter Corporation is issuing a correction for the Prismax. If the operator initiates therapy with a saved prescription and makes a change to the prescription after a disposable filter change using the same patient button, the Prismax may display values from the original prescription profile, rather than the current prescription.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/prismax-control-unit-2021-10-0

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.