Product Wiki · Recalls · Health Canada — Medical Devices

CARDIOSAVE Intra-Aortic Balloon Pump (IABP) (2018-05-08) — recall 60981

Health Canada — Medical Devices · Canada · 2018-05-25 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
60981
Date of alert
2018-05-25
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Maquet/Getinge has received complaints involving the CARDIOSAVE IABPs regarding ingress of fluids into the IABP affecting various electronic circuit boards. This situation would prevent initiation or continuation of therapy.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cardiosave-intra-aortic-balloo

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