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

Recall Z-0613-2024 — Alinity ci-series System Control Module, REF: 03R70-01

U.S. FDA — Device Enforcement · United States · 2023-05-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0613-2024
Date of alert
2023-05-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abbott Laboratories
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00380740137410
Reported risk: There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error during daily maintenance; 2) Sample Laboratory Report error; 3) Customer requests mechanism to prevent user error when creating new lots of value assigned Calibrators; 4) Error in processing tests after CCCintController encountered an error with the assay information downloaded from SCC; 5) The assay editor does not correctly check sample dilution total volume limits; 6) User-Applied Labels not adhering to Reagent Bottles; 7) ICT Module did not expire after warranty was exceeded. These performance issues could lead to erroneous results for multiple analytes.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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