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Quanta Lite ACA IgG III Kit — recall 48319

Health Canada — Medical Devices · Canada · 2012-12-28 · Type III

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Agency: Health Canada — Medical Devices
Recall identifier: 48319
Date of alert: 2012-12-28
Country / jurisdiction: Canada
Risk level: Type III
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Some kit labels have the wrong lot number for the HRP Stop Solution (Part # 508509), which is a component of the kit. Some kit labels indicate the correct lot # 003267. Other kit labels show the incorrect lot # of the HRP Stop Solution as 003627.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/quanta-lite-aca-igg-iii-kit

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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Quanta Lite ACA IgG III Kit — recall 48319

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