Product Wiki · Recalls · U.S. FDA — Device Enforcement

ADVIA 2120 REFURB DAA AUTOSAMPLER (SMN 10374454) - OUS, automated hematology analyzer Software Versions 6.10 and 6.11 — recall Z-1399-2021

U.S. FDA — Device Enforcement · United States · 2021-03-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1399-2021
Date of alert
2021-03-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10374454
Reported risk: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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