Product Wiki · Recalls · Health Canada Consumer Product Safety

Recall 63284 — STA - ImmunoDef VIII and STA-Deficient VIII (2020-03-05)

Health Canada Consumer Product Safety · Canada · 2020-04-15 · 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
63284
Date of alert
2020-04-15
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/sta-immunodef-viii-and-sta-def

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.

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.