Product Wiki · Recalls · Health Canada — Medical Devices

Remisol Advance (2019-09-16) — recall 59643

Health Canada — Medical Devices · Canada · 2019-10-03 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
59643
Date of alert
2019-10-03
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Remisol Advance archives test results and patient information on a database, which allows the use of this data for later manual review. Beckman Coulter identified a case where in a customer's database there were duplicated archived results that did not match the patient ID due to a deadlock in the database.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/remisol-advance-2019-09-16

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