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FDA Alert: Class 1 Recall of Some Mesa Biotech COVID Tests Due to Risk of False Positives/Contamination

May 11, 2022
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This is a reprint of an FDA Alert. Mesa Biotech, Inc., Recalls Certain Accula SARS-CoV-2 Tests for Risk of False Positives Caused by Contamination 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. Recalled Product Product Name: Accula SARS-CoV-2 Test Product Codes: QJR…

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Acula

May 11, 2022
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FDA Alert: Class 1 Recall on Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test

May 11, 2022
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This is a reprint of an FDA Alert. Do Not Use Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test: FDA Safety Communication May 10, 2022 The U.S. Food and Drug Administration (FDA) is warning people not to use the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test (Colloidal Gold). This test is not authorized, cleared, or approved by the FDA for distribution…

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Skipback copy

May 11, 2022
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Other-pages

May 11, 2022
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7-Other-pages

May 11, 2022
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FB-Receipts

May 11, 2022
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FB-M30s-in-Stock

May 11, 2022
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Unboxing Screenshots 1 (Facebook, May 2022)

May 11, 2022

Unboxing Screenshots (Facebook, May 2022)

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Unboxing Screenshots 3 (Facebook, May 2022)

May 11, 2022

Unboxing Screenshots (Facebook, May 2022)

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