Product Wiki · Recalls · Health Canada — Medical Devices

Instrument Manager (IM) Abbott Alinity ci-series (abdicqii) accessory… — recall 62495

Health Canada — Medical Devices · Canada · 2021-06-10 · Type II

As described by Health Canada — Medical Devices: Instrument Manager (IM) Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0004 & v8.00.0005 (2021-04-29)

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
62495
Date of alert
2021-06-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Second and any subsequent results will have an incorrect test dilution factor in Instrument Manager if the specimen transmission option is set to collated by the Abbott Diagnostics Alinity ci-series instrument and the dilution factor is different between the first and any subsequent results.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/instrument-manager-im-abbott-a

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.