Health Canada — Medical Devices · Canada · 2015-06-26 · 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 →
Archived by the issuing authority — kept for reference
Reported risk: A technical investigation has indicated that the above lot may not react strongly with all strains of listeria Monocytogenes when used in the Microbact Listeria 12L kit (MB1128A) thus making interpretation of the result more difficult than with alternate batches. Continued use of this batch may lead to negative reporting.
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.