You should report the problem directly to the manufacturer of the test. If you have witnessed or experienced a problem with a medical device, including a COVID-19 test, you should report it. Review the full CADTH report titled Self-collection of nose and throat swab samples for SARS-CoV-2 antigen testing. We reviewed these findings and continue to recommend that COVID-19 testing devices be used according to the instructions contained in the test kit. They looked at scientific literature as well as recommendations in Canadian and international jurisdictions. The Canadian Agency for Drugs and Technologies in Health (CADTH) conducted an environmental scan related to sample collection for testing during the Omicron variant. Health Canada works closely with manufacturers and public health partners to ensure the most up-to-date information is made available. If you take a sample in a different way, your test result may be inaccurate. They are written specifically for that type of kit.
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The instructions tell you how to collect a sample and take the test.
If you learned recently that a device was authorized, please allow at least 48 hours for this list to be updated. We are unable to prioritize requests for status updates at this time. Health Canada is receiving a very high volume of requests for authorization. * Point-of-care testing devices (rapid tests) and self-testing devices totals include antigen, nucleic acid (PCR) and serological testing devices.
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