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Leukotrap WB System — recall 48182

Health Canada — Medical Devices · Canada · 2013-01-07 · Type I

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Agency: Health Canada — Medical Devices
Recall identifier: 48182
Date of alert: 2013-01-07
Country / jurisdiction: Canada
Risk level: Type I
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Report of leaks in the flexible y connector leading to the donor line.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/leukotrap-wb-system

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Leukotrap WB System — recall 48182

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