Product Wiki · Recalls · Health Canada — Medical Devices

Plum Infusion Pumps (2016-03-30) — recall 55053

Health Canada — Medical Devices · Canada · 2016-04-15 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
55053
Date of alert
2016-04-15
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Some Plum 360 and Plum A+ infusion pumps were not properly calibrated during the manufacturing process. As a result, the impacted pumps can potentially produce false proximal occlusion alarms during cassette initialization (set-up of the therapy) or the alarm may be delayed in the case of a proximal occlusion during delivery (therapy).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/plum-infusion-pumps-2016-03-30

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