Medical device recalls Moderate risk

Roche Diagnostics Corporation recalls cobas p 612 pre-analytical system; Pre-analytical sample handling that includes de-capping, Aliquotting and sorting of…

Recall date
December 27, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1090-2017
FDA classification
Class II
Brand / firm
Roche Diagnostics Corporation
Sold / distributed
TX and WA

What was recalled

cobas p 612 pre-analytical system; Pre-analytical sample handling that includes de-capping, Aliquotting and sorting of samples for analysis.

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