Health Canada — Medical Devices · Canada · 2019-04-12 · Type II
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Reported risk: This voluntary recall is being conducted in response to a field corrective action from Stryker, where there is a risk of the tubing detaching from the cassette in their PneumoSure tubesets. This could result in a lack of inflation making it difficult to visualize surgical locations during procedures. The affected surgical kits from Cardinal Presource contain one of the affected Stryker tubesets in their components.
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