Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STA Satellite Automated Multi-Parameter Analyzer This system is a fully Recalled by Diagnostica Stago, Inc. Due to Following a single customer complaint that incorrect INR...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Diagnostica Stago, Inc. directly.
Affected Products
STA Satellite Automated Multi-Parameter Analyzer This system is a fully automatic clinical instrument indicated and intended for the performance of tests on human plasma, the results of which aid in the diagnosis of coagulation abnormalities or in monitoring anticoagulant therapy.
Quantity: 232 units US; 5 units Canada
Why Was This Recalled?
Following a single customer complaint that incorrect INR values were occasionally printed for PT tests, even though the primary units (seconds) were correct, the firm investigated and confirmed the potential for printing incorrect secondary units when using an external printer and the customer printout mode on the STA Satellite¿.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Diagnostica Stago, Inc.
Diagnostica Stago, Inc. has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report