Product Wiki · Recalls · Health Canada — Medical Devices

Cobas Infinity Central Lab — recall 72405

Health Canada — Medical Devices · Canada · 2022-12-23 · 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
72405
Date of alert
2022-12-23
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: The option ''rejection of external orders'' is not working as expected in Cobas Infinity Central Lab when specific pre-conditions are met simultaneously which may lead to mismatch of sample tube ID. In Canada, none of the customers are using the impacted pre-conditions, therefore they are not impacted by the issue and are informed as a preventive action. Recall start date: December 9, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cobas-infinity-central-lab

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.