Roche Diagnostics Corporation Recall: cobas b 221 AutoQC Module Complete; Catalog numbers:
Roche Diagnostics Corporation Recall: cobas b 221 AutoQC Module Complete; Catalog numbers: is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Roche Diagnostics Corporation; Product: cobas b 221 AutoQC Module Complete; Catalog numbers: 3313522001 and 3313522692 The Roche Diagnostics Omni S
| Recalling firm | Roche Diagnostics Corporation |
|---|---|
| Product | cobas b 221 AutoQC Module Complete; Catalog numbers: 3313522001 and 3313522692 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, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate. |
| Reason for recall | The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | USA ( nationwide) |
| Recall initiated | 20180222 |
| Recall number | Z-1613-2018 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
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