Product Wiki · Recalls · Health Canada — Medical Devices

Parapac Plus 310 — recall 75721

Health Canada — Medical Devices · Canada · 2024-06-21 · 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 on this page. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
75721
Date of alert
2024-06-21
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Anaesthesiology
Product type
Medical devices
Reported risk: An issue involving a Parapac Plus™ P310 ventilator, where there is potential for inadvertent tidal volume knob movement from the original setting, when set at high (1000 - 1500 ml) and low (70 - 150 ml) settings. Recall start date: June 5, 2024
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from Health Canada — Medical Devices →

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/parapac-plus-310

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.