Product Wiki · Recalls · Health Canada — Medical Devices

Acrysof Cachet Phakic Lens (2014-09-19) — recall 52472

Health Canada — Medical Devices · Canada · 2014-10-02 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
52472
Date of alert
2014-10-02
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: Alcon is voluntarily discontinuing the Cachet Phakic Lens based on data analysis from an ongoing 10-year study to evaluate the safety of the Cachet Phakic Lens in patients with myopia (near-sightedness) from -6.0 to -16.5 D vision correction. Patients with the Cachet Phakic Lens should continue with the ongoing monitoring and evaluation outlined in the current directions for use (DFU). In cases where an explant is warranted in accordance with the criteria set out in the attached DFU, Alcon will work with the treating ophthalmologist to ensure that the affected patients receive an explant without incurring out-of-pocket costs.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/acrysof-cachet-phakic-lens-201

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