Product Wiki · Recalls · Health Canada — Medical Devices

Alveogyl (2015-06-16) — recall 53869

Health Canada — Medical Devices · Canada · 2015-08-24 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
53869
Date of alert
2015-08-24
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Septodont currently distributes this device in Canada as a class 1 medical device. An internal audit has concluded that this device should be classified as a class 2 medical device. All products in the field will therefore be recalled and commercial sales stopped until the product is licensed appropriately..
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/alveogyl-2015-06-16

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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.