FDAJuly 24, 2015device
cobas Liat Analyzer, for in vitro diagnostic use.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Due to a supplier issue, the incorrect green and amber LED components were used in the manufacture of the LED printed circuit board assemblies (PCBA) in certain cobas Liat Analyzers.
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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