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Recall Observatory FDA recall evidence

Device product

S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes Analyzer; 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, urea/BUN, bilirubin, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.

Z-2330-2015

June 24, 2015

Class II

Product summary

Firm
Roche Diagnostics Operations, Inc.
Event
Event 71609
Status
Terminated
Classification
Class II
Quantity
19 affected devices of lot 21450781 were distributed in the US.
Official record key
device-enforcement:Z-2330-2015

Official wording

Reason: The affected S2 fluid packs may generate a transponder error when the fluid pack is loaded on to the cobas b 221 system. The error prevents the fluid from being recognized by the system and the instrument cannot start measurements until the affected S2 Fluid Pack is replaced.

Code information: Catalog Number: 03260925184; Lot Numbers & Exp. Dates: 1. 21450781, Exp. 08/31/2016 2. 21450887, Exp. 08/31/2016 3. 21451391, Exp. 09/30/2016

Distribution pattern: US Distribution: CT, TX, LA, ND, MI, NJ, OH, OK, PR, SC, and KY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The affected S2 fluid packs may generate a transponder error when the fluid pack is loaded on to the cobas b 221 system. The error prevents the fluid from being recognized by the system and the instrument cannot start measurements until the affected S2 Fluid Pack is replaced.