VERIFIED OFFICIAL-SOURCE INDEX

Current Medical Device Recalls in Canada – Page 2

This Canada index groups verified medical device recalls by product, hazard, official source and available identifiers.

Last updated: October 8, 2026 at 7:40 PM UTC · Official sources are checked throughout the day.

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Showing 41–46 of 46 notices · Page 2 of 2

Health Canada · August 14, 2026

Affected product: Orthopaedic Implant Components
Category: Medical device recalls
Hazard: Stryker has become aware that the devices listed in the Customer Letter were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five (5) years. Industry guidance for storage duration of UHMWPE raw material used…

Health Canada · August 14, 2026

Affected product: Endotracheal Tube, Cuffed
Category: Medical device recalls
Hazard: The 6FR suction catheter could not pass smoothly through the 2.5mm sizes of cuffed tracheal tube. This may lead to reintubations if the airway is unable to be suctioned.To date, there have been two complaints reported from united states customers where one…

Health Canada · August 11, 2026

Affected product: Omni-Tract Surgical Retractor System
Category: Medical device recalls
Hazard: Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum sterilization dry time requirements, to ensure the Omni-Tract® devices and components are properly…

Health Canada · August 7, 2026

Affected product: Bravo - Capsule Delivery System
Category: Medical device recalls
Hazard: s associated with this issue include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient. Lots with…

Health Canada · August 6, 2026

Affected product: Beckman Coulter AU Immunochemistry System - AU480 Analyzer
Category: Medical device recalls
Hazard: Beckman Coulter has determined that a software defect in AU480 chemistry analyzers using Microsoft® SQL server 2022 express may cause a DB connection error that renders alarmDB unreadable and prevents instrument startup. The issue is associated with…

Health Canada · August 6, 2026

Affected product: HEALON EndoCoat PRO
Category: Medical device recalls
Hazard: s associated with cannula insertion and provide additional clarification regarding insertion technique to support the safe and effective use of the product. This recall does not require removal or return of the product from the market. When used in accordance…