Product Wiki · Recalls · Health Canada — Medical Devices

BD Alaris Pump Module Model 8100 (2021-03-03) — recall 62252

Health Canada — Medical Devices · Canada · 2021-03-18 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
62252
Date of alert
2021-03-18
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: BD is initiating a new voluntary recall for the BD Alaris Pump Module Model 8100 due to potential lifting of the keypad, which could result in one or more keys becoming unresponsive or stuck (i.E., Constantly pressed state) due to fluid ingress. This issue may potentially result in a delay to the start of infusion or an interruption of infusion.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-alaris-pump-module-model-81

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