Product Wiki · Recalls · Health Canada — Medical Devices

Synchron Systems Cannabinoid (THC) Reagent (2019-08-31) — recall 59602

Health Canada — Medical Devices · Canada · 2019-09-20 · 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
59602
Date of alert
2019-09-20
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Studies indicate that cross-reactivity testing may not meet the claims indicated in the Cannabinoid 100 ng instructions for use (IFU) for 9 -THC or the claims indicated in the Cannabinoid 50 ng instructions for use (IFU) for Cannabinol and 9 -THC.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/synchron-systems-cannabinoid-t

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.