Dr. Howard Smith Reports

Skippack SARS-CoV-2 Antigen Rapid Test Kits Lack FDA Approval


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Vidcast: https://youtu.be/vET-yECMXZQ

The FDA and Universal Meditech Inc. now recall Skippack SARS-CoV-2 Antigen Rapid Test Kits. This product was never FDA cleared or approved before marketing. About 56,300 of these kits were sold. If you bought this product, do not use it and return it to the place of purchase for a refund. For more information, call the Universal Meditech company at 1-702-871-9888.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/universal-meditech-inc-issues-nationwide-recall-skippack-medical-lab-sars-cov-2-antigen-rapid-test

#skippack #covidtest #FDA #unapproved #recall


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Dr. Howard Smith ReportsBy Howard G. Smith MD, AM