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    <title>Food and Drug Administration on World Doctors Alliance</title>
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      <title>Innova Medical Group Recalls Unauthorized Sars Cov 2 Antigen Rapid Qualitative Test Risk False Test</title>
      <link>https://www.worlddoctorsalliance.com/blog/innova-medical-group-recalls-unauthorized-sars-cov-2-antigen-rapid-qualitative-test-risk-false-test/</link>
      <pubDate>Fri, 25 Jun 2021 15:51:12 +0100</pubDate>
      
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      <description>The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
READ HERE: US Food and Drug Administration:</description>
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