Product Wiki · Recalls · Health Canada — Medical Devices

Nitric Oxide Therapy Adapters And Connectors — recall 74141

Health Canada — Medical Devices · Canada · 2023-08-21 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
74141
Date of alert
2023-08-21
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Anaesthesiology
Product type
Medical devices
Reported risk: A single lot (74M2001125) of the one-way valve (part #50412 (pack of 5)) utilized with the Inomax dsir plus is being recalled. The one-way valve is used to prevent reverse flow into the Inomax dsir injector module from high frequency ventilators and spontaneous mask setups. The recall is being initiated due to the possibility of this lot of one-way valves sticking, by preventing or reducing the breathing circuit flow. We have no reports of serious injuries due to this issue. Recall Start Date: August 8, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/nitric-oxide-therapy-adapters-

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.

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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.