ClearanceBrief
Recall Z-1403-2021 · GKZ Counter, Differential Cell

Siemens Healthcare Diagnostics, Inc.

ADVIA 2120i Refurb Dual Aspirate (SMN 11314045) - OUS, automated hematology analyzer Software Versions 6.10 and 6.11

DateMar 5, 2021
StatusOpen, Classified
ReasonPotential Sample Identification (SID) Mismatch with14-Character Barcodes
Root causeUnder Investigation by firm
ActionSiemens Healthcare Diagnostics issued Urgent Medical Device Correction (UMDC) letter HSW21-01.A.US to US customers on March 5, 2021 via FedEx overnight delivery. An Urgent Field Safety Notice (UFSN) HSW21-01.A.OUS was issued to all OUS Siemens sites with affected customers electronically for distribution and regional reporting to their local competent authorities. Letter states reason for recall, health risk and action to take: with your Medical Director. If you are using 14-character Sample Identification (SID) barcodes: o Ensure that the Barcode Encoding Selectivity feature is enabled. Op
Quantity27 units
DistributionWorldwide 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
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K102644ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I
Siemens Healthcare Diagnostics, Nov 23, 2011
K162977ADVIA 2120i, ADVIA 2120
Siemens Healthcare Diagnostics, Aug 11, 2017