ADVIA 2120i Refurb Single Aspirate (SMN 11314044) - US, automated hematology analyzer Software Versions 6.10 and 6.11
Check against the official notice below — it lists the full affected range.
Siemens Healthcare Diagnostics has recalled one ADVIA 2120i Refurb Single Aspirate automated hematology analyzer (SMN 11314044) with software versions 6.10 and 6.11 due to a potential sample identification mismatch when using 14-character barcodes. The device was distributed nationwide in the US and to numerous countries worldwide.
The recall notice does not specify a remedy or corrective action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Reason for recall: Potential Sample Identification (SID) Mismatch with14-Character Barcodes Distribution: Worldwide distribution - US Nationwide distribution and the countries of Albania, Algeria, Angola, Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Benin, Bosnia Herzeg., Botswana, Brazil, Bulgaria, Burkina, Faso, Cambodia, Canada, Chile, Colombia, Croatia, Cura¿ao Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Fren.Polynesia, Georgia, Germany, G Quantity: 1 unit Lot/code info: Software Versions 6.10 and 6.11 UDI: 00630414237879
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.