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Bruxzir® Burs — recall 77126

Health Canada — Medical Devices · Canada · 2025-03-21 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 77126
Date of alert: 2025-03-21
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Dental
Product type: Medical devices

Reported risk: There is no defect to the products. Products were sold in Canada that are not licensed for sale in Canada. This includes a variety of dental products such as burs, abutments, dental screws, impression copying trays, etching kits, dental resins and others. These also include products manufactured by Myerson, Zest Anchors LLC, Erkodent, Airway Management Inc.and Luxcreo. Contact Prismatik Dentalcraft for further information. Recall start date: January 24, 2025

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bruxzirr-burs

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Bruxzir® Burs — recall 77126

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