Product Wiki · Recalls · Health Canada — Medical Devices

Biofire Blood Culture Identification 2 (BCID2) Panel — recall 75774

Health Canada — Medical Devices · Canada · 2025-06-03 · Type II

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
75774
Date of alert
2025-06-03
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Chemistry
Product type
Medical devices
Reported risk: Biomerieux has observed an increase in customer complaints associated with false positive Serratia marcescens results on the Biofire BCID2 panel when used in conjunction with specific lots numbers of BACT/ALERT PF Plus and BACT/ALERT FA Plus culture bottles. Recall Start Date: June 10, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/biofire-blood-culture-identifi

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.