Product Wiki · Recalls · Health Canada — Medical Devices

Custom Tubing Packs (2021-03-19) — recall 62297

Health Canada — Medical Devices · Canada · 2021-04-01 · 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
62297
Date of alert
2021-04-01
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The packs listed above contain component 700000172 which is a bacterial filter. DEKRA Certification GmbH (MCP's notified body) issued the decision letter regarding the design dossier review of Customized Tubing Sets (CTPs) under MDD recertification. Due to the insufficient evidence regarding the shelf life of this component, the overall shelflife of the finished tubing packs containing this component must be reduced by one year.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/custom-tubing-packs-2021-03-19

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.