FDADecember 18, 2014device

cobas 4800 KRAS AMP/DET 24T CE-IVD Mutation Test; CE-IVD 5852170190. Intended for the identification of mutations in codons 12,13 and 61 of the KRAS Gene in DNA derived from formalin-fixed paraffin-embedded human colorectal and non-small cell lung cancer tissues.

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

The hazard

cobas KRAS Mutation Kit T10786 is generating invalid results for the Mutant Control and/or KRAS Calibrator.

What to do

FDA enforcement status: Terminated

Brands named

roche molecular systemsrocheroche molecular

Recall history

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

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