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Recall Variant II Turbo Hemoglobin System, Bio-Rad

Product group In-vitro diagnostics
Reference 04195/07

Corrective action and recall of Bio-Rad for the Variant II Turbo Hemoglobin System 270-2600 (software version CDM 3.6T) because of erroneous results. Customers were informed about the problem and how to avoid it. A new software version will be developed.

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