Product Wiki · Recalls · Health Canada — Medical Devices

PrisMax Control Unit (2021-01-13) — recall 62045

Health Canada — Medical Devices · Canada · 2021-01-29 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
62045
Date of alert
2021-01-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Baxter Corporation is issuing an urgent medical device correction to the users of the Prismax control unit, due to the variability in performance of the tubing in the ARPS (automatic repositioning system) pump assembly which may lead to alarm situations during a system self-test and during therapy.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/prismax-control-unit-2021-01-1

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