Product Wiki · Recalls · Health Canada — Medical Devices

ARCHITECT I System - DHEA-S Assay (2017-12-19) — recall 57973

Health Canada — Medical Devices · Canada · 2018-01-08 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
57973
Date of alert
2018-01-08
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Abbott has identified that falsely elevated results may be obtained when using the ARCHITECT DHEA-S Assay with samples from infants up to 60 days old. The specific cause of the elevated results is currently under investigation. Although falsely elevated results have only been observed with samples from infants up to 60 days old, the expected values representative data for children up to 10 years old provided in the ARCHITECT DHEA-S reagent insert should not be used as these reference ranges are being reviewed as part of the investigation. All in-date lots of current reagent inventory are impacted.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/architect-system-dhea-s-assay-

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