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Dose IQ Safety Software — recall 73759

Health Canada — Medical Devices · Canada · 2023-06-07 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
73759
Date of alert
2023-06-07
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: Baxter Corporation is issuing an urgent medical device correction due to a defect in the Dose IQ Safety Software used with Novum IQ Large Volume Pump, resulting in an invalid initial setting for the air-in-line threshold for any new care area created in which none of the settings are changed. Recall start date: May 29, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/dose-iq-safety-software

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