| 000 | 00000nam 2200000zi 4500 |
| 001 | 9.953092 |
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| 003 | CaOODSP |
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| 005 | 20250910143430 |
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| 006 | m o d f |
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| 007 | cr ||||||||||| |
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| 008 | 250710e202507##onc ob f000 0 eng d |
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| 020 | |a9780660780887 |
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| 040 | |aCaOODSP|beng|erda|cCaOODSP |
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| 043 | |an-cn--- |
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| 086 | 1 |aH139-93/2025E-PDF |
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| 245 | 00|aGuide for recalling medical devices (GUI-0054). |
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| 264 | 1|aOttawa : |bHealth Canada = Santé Canada, |cJuly 2025. |
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| 264 | 4|c©2025 |
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| 300 | |a1 online resource (54 pages) |
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| 336 | |atext|btxt|2rdacontent |
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| 337 | |acomputer|bc|2rdamedia |
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| 338 | |aonline resource|bcr|2rdacarrier |
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| 500 | |aIssued also in French under title: Guide sur les rappels d'instruments médicaux (GUI-0054). |
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| 504 | |aIncludes bibliographical references. |
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| 520 | |a"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. |
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| 650 | 0|aMedical instruments and apparatus|xSafety regulations|zCanada. |
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| 650 | 0|aProduct recall|zCanada. |
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| 710 | 1 |aCanada. |bHealth Canada, |eissuing body. |
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| 775 | 08|tGuide sur les rappels d'instruments médicaux (GUI-0054).|w(CaOODSP)9.953093 |
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| 856 | 40|qPDF|s1.46 MB|uhttps://publications.gc.ca/collections/collection_2025/sc-hc/H139-93-2025-eng.pdf |
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| 856 | 4 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/problem-reporting/medical-devices-recall-guide-0054.html |
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| 986 | |a250132 |
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