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Recall for TheraScreen K-RAS Mutation Kit, DxS Ltd. / Roche Diagnostics

2009.10.05

Product group In-vitro diagnostics
Reference 03493/09

Recall of DxS Ltd. / Roche Diagnostics for TheraScreen K-RAS Mutation Kit because of invalid Mixed Standard. The customers were requested to discontinue use and discard the lots affected.

Recall for TheraScreen K-RAS Mutation Kit, DxS Ltd. / Roche Diagnostics , Download_VeroeffentlichtAm_EN PDF, 28KB, File does not meet accessibility standards