Product Wiki · Recalls · Health Canada — Medical Devices

Architect C16000/C4000 System - Processing Modules (2017-10-04) — recall 57282

Health Canada — Medical Devices · Canada · 2017-10-13 · 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
57282
Date of alert
2017-10-13
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Abbott has become aware that the Peristaltic Head tubing placed on the Architect has the possibility to leak due to a manufacturing issue associated with the tubing connector. This tubing was not original to Architect, but installed during a service visit that occurred between June 16, 2017 and July 20, 2017. Peristaltic Head tubing is used on Architect clinical chemistry instruments as part of waste aspiration during the cuvette cleaning process.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/architect-c16000c4000-system-p

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.