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Guide for recalling medical devices (GUI-0054).: H139-93/2025E-PDF

"Recalling a product generally means removing it from sale or correcting a device. In Canada, actions such as notifying users of a potential problem or supplying different labelling for a medical device are also considered recalls. This guide is for manufacturers, importers and distributors who work with medical devices"--Purpose, page 6.

Permanent link to this Catalogue record:
publications.gc.ca/pub?id=9.953092&sl=0

Publication information
Department/Agency
  • Canada. Health Canada, issuing body.
TitleGuide for recalling medical devices (GUI-0054).
Publication typeMonograph
Language[English]
Other language editions[French]
FormatDigital text
Electronic document
Note(s)
  • Issued also in French under title: Guide sur les rappels d'instruments médicaux (GUI-0054).
  • Includes bibliographical references.
Publishing information
  • Ottawa : Health Canada = Santé Canada, July 2025.
  • ©2025
Description1 online resource (54 pages)
ISBN9780660780887
Catalogue number
  • H139-93/2025E-PDF
Departmental catalogue number250132
Subject terms
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