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Corrective action for RAPIDPoint® 400 Series, RAPIDPoint® 500 and RAPIDLab® 1200 Series Analyzers, Siemens

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05828/13

Corrective action from Siemens for RAPIDPoint® 400 Series, RAPIDPoint® 500 and RAPIDLab® 1200 Series Analyzers due to a risk for sample misidentification. Customers were again informed about the problem.

See also BfArM case-No. 5828/13 from 2013-12-06

Corrective action for RAPIDPoint® 400 Series, RAPIDPoint® 500 and RAPIDLab® 1200 Series Analyzers, Siemens , Download_VeroeffentlichtAm_EN PDF, 29KB, File does not meet accessibility standards