FDADecember 21, 2021device

C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalog # EIA-1293

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

ODs of the standards too low(< 0.6 ODmax) may cause invalid runs, delayed patient results are possible

What to do

FDA enforcement status: Terminated

Brands named

drg

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalog # EIA-1293 — Recall Details · AllClear