Product Wiki · Recalls · Health Canada — Medical Devices

Alinity i and Alinity c Processing Module (2019-03-04) — recall 59225

Health Canada — Medical Devices · Canada · 2019-03-15 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
59225
Date of alert
2019-03-15
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Abbott has identified that the safety interlock covering the septum piercing probes within the bulk solution bottle holder may not deploy when a bulk solution bottle is removed from the Alinity ci-series.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/alinity-and-alinity-c-processi

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