Product Wiki · Recalls · Health Canada — Medical Devices

ProTaper GOLD F1 21mm (2018-08-07) — recall 58327

Health Canada — Medical Devices · Canada · 2018-08-31 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
58327
Date of alert
2018-08-31
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: As per Health Hazard Evaluation (HHE-341): Risk level is II as it causes additional/unplanned interventions or corrections during the course of a treatment or after a treatment with no health risk to the patient. There is no long term health impact on the patient. This is a type III recall in Canada.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/protaper-gold-f1-21mm-2018-08-

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.

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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.