FDAMarch 15, 2016device

cobas¿ EGFR Mutation Test, v2 and cobas¿ cfDNA Sample Preparation Hungarian Translation Instructions for Use

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

The hazard

An error was found within the Hungarian translations of the cobas¿ EGFR Mutation Test v2 Instructions for Use (M/N 07340761001-01HU, Doc Rev. 1.0, Dated 08/2015) and the cobas¿ cfDNA Sample Preparation Kit Instructions for Use (M/N 07573758001-01HU, Doc. Rev. 1.0, Dated 05/2015).

What to do

FDA enforcement status: Terminated

Brands named

roche molecular systemsrocheroche molecular

UPCs

0724856319007247737190

Recall history

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

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