Product Wiki · Recalls · Government of Canada recall portal

Diagnostic tests — recall 49054

Government of Canada recall portal · Canada · 2013-02-08

As described by Government of Canada recall portal: Diagnostic tests manufactured by IND Diagnostic or other private label manufacturers

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
Government of Canada recall portal
Recall identifier
49054
Date of alert
2013-02-08
Country / jurisdiction
Canada
Risk type
recall
Product category
Medical devices
Product type
Communications and Public Affairs Branch
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Health Canada today suspended all medical device licences issued to and associated with IND Diagnostic of Delta, B.C., under its powers in the Food and Drugs Act, because of concerns about the company's management systems and distribution practices. The suspension means the devices can no longer be legally sold in Canada by any person. Health Canada's decision to suspend these licences is not based on an identified issue with the safety and effectiveness of any particular device.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/diagnostic-tests-manufactured-

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.