Product Wiki · Recalls · Health Canada — Medical Devices

Datascope Corp. Intra Aortic Balloon Pump (2017-07-20) — recall 57210

Health Canada — Medical Devices · Canada · 2017-07-28 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
57210
Date of alert
2017-07-28
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Manufacturer has determined that condensation in the drain line tubing may lead to a false blood detection alarm activating when no blood is present. Also liquid spills, such as saline, can create bridges of resistance between the circuit components, causing the circuit not to function as intended. This can impact initiation or continuation of therapy.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/datascope-corp-intra-aortic-ba

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