Product Wiki · Recalls · Health Canada — Medical Devices

Biotrin Control Parvovirus B19 IgM (2014-01-07) — recall 50641

Health Canada — Medical Devices · Canada · 2014-02-11 · 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 above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
50641
Date of alert
2014-02-11
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Internal investigation confirmed that C of A of Biotrin Control Parvovirus B19 IGM is reporting an incorrect negative control range for the Liaison XL application when used in combination with Biotrin Parvovirus B19 IGM kit.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/biotrin-control-parvovirus-b19

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.