Stago recalls STA-Fibrinogen 5 kit (model 00674) due to potential contamination of anticoagulant reagents in UFH and LMWH treatments. Affected users should contact Stago for guidance.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Stago is recalling its STA-Fibrinogen 5 kit (model : 00674) because it could contaminate anticoagulant reagents used in blood thinners like heparin and low molecular weight heparin. This poses a risk for incorrect blood clotting tests and potential treatment errors.
The kit could contaminate anticoagulant reagents when used with certain blood thinners (heparin and low molecular weight heparin). This might lead to incorrect blood clotting test results, potentially causing treatment errors.
Healthcare professionals using the STA-Fibrinogen 5 kit for blood clotting tests with Stago analyzers are most at risk. Patients receiving anticoagulant therapy using this kit may also be affected.
Check for the model number 00674 on the STA-Fibrinogen 5 kit. The kit is intended for use with Stago analyzers like STA-R, STA Compact, and STA Satellite.
Reach out to Stago directly to get specific instructions on handling the recalled kit and potential next steps.
The recall affects healthcare professionals using the kit for blood tests. Patients receiving anticoagulant therapy with this kit may be at risk, but the official notice does not specify direct patient impact.
Look for the model number 00674 on the STA-Fibrinogen 5 kit, which is intended for use with Stago analyzers like STA-R, STA Compact, and STA Satellite.
Contact Stago directly for specific guidance on handling the recalled kit and potential next steps.
We’ve drafted a message you can send Stago to request your refund or repair — edit it as you like.
Subject: Recall Z-2476-2025 — Stago Stago Hello, I own a Stago that is covered by recall Z-2476-2025 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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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.
