Product Wiki · Recalls · Health Canada Consumer Product Safety

Recall 60786 — iQ200 Sprint and Elite Automated Urine Microscopy Analyzer, iQ200 Select Urinanlysis System - Analyzer, iQ200 Elite Plus and Pro, iQ Select Plus and Pro, iQ Sprint Plus and Pro (2018-02-26)

Health Canada Consumer Product Safety · Canada · 2018-04-03 · Type II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
Health Canada Consumer Product Safety
Recall identifier
60786
Date of alert
2018-04-03
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Medical devices
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/iq200-sprint-and-elite-automat

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.