Stago STA Satellite Recall: Risk of Contamination in Blood Tests

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Recalling firmDiagnostica Stago, Inc.5 Century Dr · Parsippany, NJ 07054-4607

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Stago is recalling all STA Satellite blood analyzers because they might contaminate anti-Xa blood tests with fibrinogen reagents used in some anticoagulant treatments. This could lead to inaccurate test results for patients using these specific medications.

Why it’s dangerous

The STA Satellite analyzer might mix fibrinogen reagents from different tests, contaminating anti-Xa blood tests. This could cause inaccurate results for patients on anticoagulant medications like heparin or low molecular weight heparin.

Who’s affected

Healthcare facilities using the STA Satellite blood analyzer are most affected. Patients using anti-Xa tests with fibrinogen reagents in UFH or LMWH treatments may be impacted.

How to tell if you have this one

Check for the product code on the device or its packaging. The STA Satellite is a fully automated blood analyzer sold with all software versions and reference numbers.

Brand
Stago
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Look for the product code on the device or its packaging to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The STA Satellite might contaminate anti-Xa blood tests with fibrinogen reagents used in some anticoagulant treatments, potentially causing inaccurate results.

What should I do if I have this product?

The recall doesn't specify a remedy, so check with Stago directly for guidance.

Is there a risk of serious injury?

The recall doesn't mention serious injury risks, so it's considered low risk.

Take action

Contact Stago

We’ve drafted a message you can send Stago to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2473-2025 — Stago Stago

Hello,

I own a Stago that is covered by recall Z-2473-2025 from Stago.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2473-2025 (July 21, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2473-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Diagnostica Stago, Inc. recalls STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop

Lower-risk recall