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Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche

2006.01.10

Product group In-vitro diagnostics
Reference 02832/05

Corrective action and Recall of Roche for Omni S system versions 2, 4 and 6 with CO-oximetry because of a malfunction of the QC -limits for hemoglobin derivatives. Customers were informed informed about the problem and how to avoid it. A new software version will be developed.

Advisory Notice is only available in German language.

Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche , Download_VeroeffentlichtAm_EN PDF, 104KB,

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