Product Wiki · Recalls · Health Canada — Medical Devices

Dimension Vista System – Urinary / Cerebrospinal Fluid Protein Spray — recall 48222

Health Canada — Medical Devices · Canada · 2013-01-07 · Type III

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
48222
Date of alert
2013-01-07
Country / jurisdiction
Canada
Authority classification
Type III
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: There is an increase in the rate of absorbance errors with the Dimension Vista Urinary/Cerebrospinal Fluid Protein (UCFP) flex reagent cartridge during calibration. Patient results are not impacted, but may be delayed.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/dimension-vista-system-urinary

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.