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

Recall Z-2475-2025 — STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparins by measuring their

U.S. FDA — Device Enforcement · United States · 2025-07-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2475-2025
Date of alert: 2025-07-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Diagnostica Stago, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 03607450011791

Reported risk: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

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.

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