Product Wiki · Recalls · Health Canada — Medical Devices

Hemoconcentrator Set (2020-11-05) — recall 61843

Health Canada — Medical Devices · Canada · 2020-11-20 · 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
61843
Date of alert
2020-11-20
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Some quarantined tubing sets with a hemoconcentrator have been released to the market. The products were subjected to an unknown storage temperature for two days during transportion to the distribution center. Taking into consideration the product risks due to storage at temperature higher then recommended, the following potential health consequences (harms) could occur: - ischemia, infection, user inconvenience.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/hemoconcentrator-set-2020-11-0

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.