FDAFebruary 22, 2018device

cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, ure...

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

The hazard

The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.

What to do

FDA enforcement status: Terminated

Brands named

roche diagnosticsroche

UPCs

04015630018307

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →