Product Wiki · Recalls · Health Canada — Medical Devices

COBAS 6800, 8800 (2019-06-13) — recall 59787

Health Canada — Medical Devices · Canada · 2019-07-19 · 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
59787
Date of alert
2019-07-19
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The processing transfer heads can, in certain conditions, leak on the processing module deck, heating station and separation station, which could cause invalid results, false positives or over-quantified results as a consequence of cross contamination of samples.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cobas-6800-8800-2019-06-13

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.