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

Recall Z-1531-2014 — IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND), REF LKAO1, SMN 10381158, IVD, 100 test kit size --- Siemens Healthcare Diagnostics Products Ltd. Llanberis, Gwynedd, LL55 4EL, UK For in vitro diagnostic use with the IMMULITE/IMMULITE 1000 and 2000 Systems Analyzers for the quantit

U.S. FDA — Device Enforcement · United States · 2013-12-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1531-2014
Date of alert
2013-12-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10381158
Reported risk: Siemens Healthcare Diagnostics confirmed over-recovery of samples with concentrations greater than 5.5 ng/mL with the IMMULITE/IMMULITE 1000 and IMMULITE 2000/IMMULITE 2000 XPi Androstenedione assays (LKAO1, L2KAO2). Siemens has determined that these lots are linear up to a concentration of 5.5 ng/mL, instead of 10 ng/mL as stated in the Instructions for Use (IFU). Quality Control materials at concentrations between 5.5 and 10 ng/mL will detect this issue.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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