Product Wiki · Recalls · Health Canada — Medical Devices

Orise Gel Pack and Procedure Kit — recall 72503

Health Canada — Medical Devices · Canada · 2022-12-30 · Type II

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
72503
Date of alert
2022-12-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Ear, nose and throat - General and plastic surgery - General hospital and personal use
Product type
Medical devices
Reported risk: Boston Scientific (BSC) initiated a field action in October 2022, communicating that remnant orise gel post-procedure can cause a foreign body reaction, appearing as mass formations and submucosal distortions. Since this time, BSC has become aware of additional events leading to unnecessary medical and surgical intervention. As a result, BSC now believes the occurrence is potentially higher than anticipated, therefore, this product is being removed from the market. Recall start date: December 15, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/orise-gel-pack-and-procedure-k

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.