Health Canada — Medical Devices · Canada · 2026-02-26 · Type II
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Dental - General and plastic surgery - General hospital and personal use
Product type
Medical devices
Reported risk: The recall must be done due to misclassification which led to the sale of unlicensed medical devices. Therefore, no real or potential defectiveness is suspected. Nevertheless, users should stop using the refill tips.
Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.
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.