Product Wiki · Recalls · Health Canada — Medical Devices

Atlantis Abutments Titanium and Atlantis Abutment Gold-Shaded… — recall 59595

Health Canada — Medical Devices · Canada · 2019-09-20 · Type II

As described by Health Canada — Medical Devices: Atlantis Abutments Titanium and Atlantis Abutment Gold-Shaded Titanium (2019-08-30)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
59595
Date of alert
2019-09-20
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Due to a manufacturing failure the affected abutments have been machined with an incorrect cone. This cone is part of the interface of the implant type the abutment is intended be placed on and ensure the secure seat onto the implant.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/atlantis-abutments-titanium-an

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.