Drugs & medicalClass II

Diagnostica Stago, Inc. recalls STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent for reagents and…

Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1%

Read the official notice →
Date
2025-06-25
Country
United States
Brand
Diagnostica Stago
Product
STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent for reagents and…
Classification
Class II
Units
The affected lot was distributed to customers in various US states in October…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Diagnostica Stago recalls

  1. 2026-03-25
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    Diagnostica Stago, Inc. recalls Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: in vitro diagnostic. The…

    After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.

    FDA · DeviceDiagnostica Stago, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Singapore,…Official notice →
  3. 2026-03-11
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    Diagnostica Stago, Inc. recalls Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description:…

    The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.

    FDA · DeviceDiagnostica Stago, Inc.Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice →
  5. 2026-01-21
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    Diagnostica Stago, Inc. recalls Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of…

    Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results.

    FDA · DeviceDiagnostica Stago, Inc.Worldwide - US Nationwide distribution in the states of AL, CA, FL, GA, HI,…Official notice →
  7. 2025-10-22
  8. US
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    Diagnostica Stago, Inc. recalls Product: STA Liatest D-Di; REF: 00515;

    A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.

    FDA · DeviceDiagnostica Stago, Inc.Worldwide distribution- US Nationwide and the country of Canada.Official notice →
  9. 2025-09-03
  10. US
    Drugs & medicalClass II

    Diagnostica Stago, Inc. recalls 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 STA…

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

    FDA · DeviceDiagnostica Stago, Inc.Worldwide - US Nationwide distribution in the states of AL, AZ, CA, CO, FL,…Official notice →
  11. 2023-05-17
  12. US
    Drugs & medicalClass II

    Diagnostica Stago, Inc. recalls STA Compact Automated Multi-Parametric Analyzer, Reference Numbers 58602 and 58612

    An internal investigation identified a bug in this firmware version, resulting in the following:Intermittent shortened coagulation times and an increased frequency of occurrence of a technical error reported by the…

    FDA · DeviceDiagnostica Stago, Inc.US Nationwide distribution in the states of IL, MA, MN, NE, TX, and WI.Official notice →
All 8 Diagnostica Stago recalls →

Other drugs & medical recalls in the United States

  1. 2025-07-02
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  4. 2025-06-26
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    BALT USA, LLC recalls Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694…

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See all drugs & medical recalls →