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Hybrid Hydrophilic Microguidewire — recall 82279

Health Canada — Medical Devices · Canada · 2026-07-03 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 82279
Date of alert: 2026-07-03
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Neurology
Product type: Medical devices

Reported risk: Performance variability affecting the hydrophilic coating of Hybrid007 guidewires in specific lots may increase friction during microcatheter navigation. This may require guidewire replacement to complete the procedure, potentially prolonging procedure time and increasing the risk of procedure-related complications.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/hybrid-hydrophilic-microguidew

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Hybrid Hydrophilic Microguidewire — recall 82279

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