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Vitek® 2 Ast-N391 — recall 64421

Health Canada — Medical Devices · Canada · 2022-08-02 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 64421
Date of alert: 2022-08-02
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices

Reported risk: Some cartons of the lot of Vitek 2 Ast cards have been identified as impacted by a card and/or card label mix issue during production at the manufacturing site. The card and label of the card are incorrect and are from another Vitek 2 ID or AST reference and lot number. Recall start date: July 25, 2022

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vitekr-2-ast-n391

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Vitek® 2 Ast-N391 — recall 64421

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