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All Recalls

Every Diagnostica Stago, Inc. Recall

Sorted by most recent. Click any recall for full details.

17 recalls
High RiskFDA
Diagnostica Stago, Inc.
Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: The STA¿ - Liatest ¿ ...
Diagnostic Devices·34,000 affected·Feb 5, 2026
High RiskFDA
Diagnostica Stago, Inc.
Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum...
Medical Devices·438 affected·Dec 15, 2025
High RiskFDA
Diagnostica Stago, Inc.
Product: STA Liatest D-Di; REF: 00515;
Medical Devices·12,740 affected·Sep 12, 2025
High RiskFDA
Diagnostica Stago, Inc.
STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and ST...
Diagnostic Devices·116,600 affected·Jul 21, 2025
High RiskFDA
Diagnostica Stago, Inc.
STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop analyzer capable o...
Diagnostic Devices·3,650 affected·Jul 21, 2025
High RiskFDA
Diagnostica Stago, Inc.
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 S...
Diagnostic Devices·126,200 affected·Jul 21, 2025
High RiskFDA
Diagnostica Stago, Inc.
STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Fibrinogen 5 kit is intended for use with the analyzers of the STA-R, STA ...
Medical Devices·829,800 affected·Jul 21, 2025
High RiskFDA
Diagnostica Stago, Inc.
STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent for reagents and...
Diagnostic Devices·939 affected·May 21, 2025
High RiskFDA
Diagnostica Stago, Inc.
STA SYSTEM CONROL N + P (ref. 00678)
Medical Devices·5,437 affected·Nov 18, 2019
High RiskFDA
Diagnostica Stago, Inc.
Staclot LA 20 (REF 00594) The Staclot¿ LA and Staclot¿ LA 20 test kits are reagent systems designed for the qualitative detection of ...
Diagnostic Devices·22,342 affected·Nov 14, 2018
High RiskFDA
Diagnostica Stago, Inc.
Diagnostica Stago STA N¿oplastine¿ CI, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. REF: 0...
Diagnostic Devices·5 affected·Jul 24, 2018
High RiskFDA
Diagnostica Stago, Inc.
Diagnostica Stago STA N¿oplastine¿ CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. ...
Diagnostic Devices·24,043 affected·Jul 24, 2018
High RiskFDA
Diagnostica Stago, Inc.
STA - Neoplastine¿ Cl Plus ¿ (ref. 00606) Product Usage: Manual or automated determination of the prothrombin time (PT).
Medical Devices·0 affected·Oct 25, 2017
High RiskFDA
Diagnostica Stago, Inc.
Neoplastine¿ Cl Plus ¿ (ref. 00375) Product Usage: Manual or automated determination of the prothrombin time (PT).
Medical Devices·0 affected·Oct 25, 2017
High RiskFDA
Diagnostica Stago, Inc.
STA - Neoplastine¿ Cl ¿ (ref. 00605) Product Usage: Manual or automated determination of the prothrombin time (PT).
Medical Devices·0 affected·Oct 25, 2017
High RiskFDA
Diagnostica Stago, Inc.
Neoplastine¿ Cl Plus @ (ref.00374) Product Usage: Manual or automated determination of the prothrombin time (PT).
Medical Devices·1,636 affected·Oct 25, 2017
High RiskFDA
Diagnostica Stago, Inc.
Vial Label: 1) LIATEST VWF:Ag Buffer - 5 ml Diagnostica Stago 2) LIATEST VWF:Ag Latex + 4 ml R3 Diagnostica Stago 3) LIATEST VWF...
Diagnostic Devices·2,901 affected·Jan 28, 2013