Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls

6 recalls on record · latest: November 1, 2018

Official U.S. recall history for Clark Laboratories, Inc. (dba,Trinity Biotech USA), compiled from official government records.

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Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls ultra2 Genesys Variants Analyzer, REF 03-01-0045 intended to be used with automated high performance liquid chromatogra…

November 1, 2018 · Medical device recalls Moderate risk lack of 510K

Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls Genesys 2 Reagent, REF 01-03-0022 intended to be used with automated high performance liquid chromatography (HPLC) syst…

November 1, 2018 · Medical device recalls Moderate risk lack of 510K

Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls Genesys Analytical Column, REF 01-05-0017 intended to be used with automated high performance liquid chromatography (HP…

November 1, 2018 · Medical device recalls Moderate risk lack of 510K

Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls Genesys 1 Reagent, REF 01-03-0020 intended to be used with automated high performance liquid chromatography (HPLC) syst…

November 1, 2018 · Medical device recalls Moderate risk lack of 510K

Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls Genesys Diluent Reagent, REF 01-03-0019 intended to be used with automated high performance liquid chromatography (HPLC…

November 1, 2018 · Medical device recalls Moderate risk lack of 510K

Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls Trinity Biotech Captia Measles IgM, REF/Product Code 2326060,Test Kit for 96 Determinations, IVD

July 11, 2016 · Medical device recalls The product lot failed to meet QC acceptance criteria during stability testing.…