Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and differentiation Recalled by Versea Diagnostics LLC Due to Products may have been distributed to customers other...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Versea Diagnostics LLC directly.
Affected Products
FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, plasma (sodium EDTA) and fingerstick whole blood. Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. (CLIA Waived Laboratories)
Quantity: 563,290 in total
Why Was This Recalled?
Products may have been distributed to customers other than laboratories certified under the Clinical Laboratory Improvement Amendments as stipulated in the Emergency Use Authorization.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Versea Diagnostics LLC
Versea Diagnostics LLC has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report