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.
FDA Recall Z-0252-2013 · Posted 2012-11-06
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Recalling FirmDiagnostica Stago, Inc.
Recall StatusTerminated
Product CodeJPA
Date Initiated2012-06-15
Date Terminated2013-07-19
Product Quantity232 units US; 5 units Canada
Reason for Recall
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.
Firm Action
Diagnostica Stago sent an Urgent Field Safety Notice dated June 12, 2012, to all affected customers via email return receipt requested on June 15, 2012. Customers were instructed to follow the instructions in the notification and complete the Customer Verification form and return to the Hotline by fax to 973-644-9348. For additional information, customers were instructed to contact the Hotline at 800-725-0607.
For questions regarding this recall call 973-631-1200, ext 2044.
Root Cause
Software design
Distribution Pattern
Worldwide Distribution - USA (nationwide) and Canada
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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