Product Wiki · Recalls · Health Canada — Medical Devices

Amia Automated PD System - Cycler (2018-07-15) — recall 58644

Health Canada — Medical Devices · Canada · 2019-01-31 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58644
Date of alert
2019-01-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Baxter Corporation has identified a potential failure with the Amia cycler where the power cord socket can become loose or detached when the power cord is unplugged from the back of the cycler. To address this issue, Baxter will be inspecting and repairing any loose power cord sockets during the next Amia cycler service. The Amia cyclers may continue to be used, and do not need to be returned at this time.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/amia-automated-pd-system-cycle

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.