Product Wiki · Recalls · Health Canada — Medical Devices

AMMONIA ULTRA REAGENT (2015-09-28) — recall 54274

Health Canada — Medical Devices · Canada · 2015-10-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
54274
Date of alert
2015-10-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Due to a manufacturing issue with ammonia ultra reagent, List Number 6K89-30, Lot 50083Y600 is being removed from use. This lot is producing results below the linear range of the assay for samples that have been collected in sodium or lithium heparin tubes. Quality control results are not affected.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ammonia-ultra-reagent-2015-09-

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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