Product Wiki · Recalls · Health Canada — Medical Devices

WALLSTENT Endoprosthesis Tracheobronchial and Tracheobronchial… — recall 57749

Health Canada — Medical Devices · Canada · 2017-12-21 · Type III

As described by Health Canada — Medical Devices: WALLSTENT Endoprosthesis Tracheobronchial and Tracheobronchial Endoprosthesis with Unistep Plus Delivery System (2017-12-04)

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
57749
Date of alert
2017-12-21
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: Certain WALLSTENT RP Endoprosthesis and WALLSTENTT Endoprosthesis Stent Systems were shipped with labeling that includes indications for venous and transjugular intrahepatic portosystemic shunt (tips), neither of which are authorized by Health Canada
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/wallstent-endoprosthesis-trach

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