Ihealthlabs at home covid-19 antigen rapid test was defective and not working properly.Test kit package was supposed to contain 2 tests but only contained 1.The 1 test kit did not have sufficient fluid in the tube of extraction buffer to be usable.Test kit info: gtin(b)(4), lot no.(10): 211co21220, serial no.(b)(4).Use by(17):2022-06-19.Tube of extraction fluid lot no: cvd2121216 tube of extraction fluid use by: 2023-12-12.Unable to report directly to company due to security problems with the company's contact us web page.Fda safety report id # (b)(4).
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