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

Recall Z-1672-2025 — DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 Software versions: V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in sam

U.S. FDA — Device Enforcement · United States · 2025-03-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1672-2025
Date of alert
2025-03-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beckman Coulter Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14987666545058
Reported risk: The reason for the recall is incorrect sample barcode identification and processing errors that result in the reporting of erroneous and delayed results.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.