Corrective action and recall of for the Advia 2110 Hematology System from Bayer Healthcare
2006.07.21
Product group In-vitro diagnostics
Reference 01658/06
Corrective action and recall of Bayer Healthcare for the Advia 2110 Hematology System (Software versions V5.0.6, V5.2.7 and V5.1.1) because of an erroneous sample dilution. Customers were informed about the problem and how to avoid it. A new software version has been developed.