00000nam 2200000zi 4500 9.953092 CaOODSP 20250910143430 m o d f cr ||||||||||| 250710e202507##onc ob f000 0 eng d 9780660780887 CaOODSP eng rda CaOODSP n-cn--- H139-93/2025E-PDF Guide for recalling medical devices (GUI-0054). Ottawa : Health Canada = Santé Canada, July 2025. ©2025 1 online resource (54 pages) text txt rdacontent computer c rdamedia online resource cr rdacarrier Issued also in French under title: Guide sur les rappels d'instruments médicaux (GUI-0054). Includes bibliographical references. "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. Medical instruments and apparatus Safety regulations Canada. Product recall Canada. Canada. Health Canada, issuing body. Guide sur les rappels d'instruments médicaux (GUI-0054). (CaOODSP)9.953093 PDF 1.46 MB https://publications.gc.ca/collections/collection_2025/sc-hc/H139-93-2025-eng.pdf HTML N/A https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/problem-reporting/medical-devices-recall-guide-0054.html 250132