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Ansh Labs, LLC: Medical Device Recalls in 2021

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Ansh Labs, LLC in 2021. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2021
  • AnshLabs - SARS-CoV2 IgM ELISA (u-Capture), IVD, REF: AL-1002, kit contents, Ab PLATE 1 X ! Plate, IgM Sample DIL 1 x 100 mL, ENZ CONJ CONC 1 x 1.5 mL, Calibrators A-C 3 x 1.2 mL, CONJ DIL 1 X 12 mL, Stop SOLN 1 X 12 mL, TMB SOLN 1 X 12 mL, WASH CONC A 1 X 60 mL, (01)00853592008219 - Product Usage: intended for the qualitative detection of IgM antibodies in serum collected from the individuals suspected with signs and symptoms of COVID-19 infection by their healthcare provider.
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