Product Wiki · Recalls · Health Canada — Medical Devices

Combi Loop Sling (2019-01-24) — recall 58721

Health Canada — Medical Devices · Canada · 2019-02-15 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58721
Date of alert
2019-02-15
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Arjo has received a limited number of complaints identifying a potential malfunction with the orange loop stitching of the Combi Slings. If the failure of the loop is not detected prior to transfer, as per information provided in the instructions for use, this may lead to a patient fall potentially causing major trauma or head injury.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/combi-loop-sling-2019-01-24

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