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Allura XPER Products — recall 49391

Health Canada — Medical Devices · Canada · 2012-06-11 · Type III

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Agency: Health Canada — Medical Devices
Recall identifier: 49391
Date of alert: 2012-06-11
Country / jurisdiction: Canada
Risk level: Type III
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: There is a performance issue during initializing of application that could lead to the unavailability of the follow C-Arc function. As a consequence the function cannot be used but this will not impact patient safety.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-products

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Allura XPER Products — recall 49391

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