Product Wiki · Recalls · Health Canada — Medical Devices

Oscar 2, ABP/CBP System (2020-03-31) — recall 61226

Health Canada — Medical Devices · Canada · 2020-05-08 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
61226
Date of alert
2020-05-08
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Suntech Medical Instruments, Inc. received a complaint (COM-000123) stating that the unit displayed 12.0 Instead on 120. Investigation has revealed that an erroneous configuration setting was applied to the devices during production.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/oscar-2-abpcbp-system-2020-03-

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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