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Recall Observatory FDA recall evidence

Device product

STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference Numbers 59013 and 59026

Z-1575-2023

March 22, 2023

Class II

Product summary

Firm
Diagnostica Stago, Inc.
Event
Event 92007
Status
Ongoing
Classification
Class II
Quantity
6 analyzers
Official record key
device-enforcement:Z-1575-2023

Official wording

Reason: 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 analyzer (error 13).

Code information: UDI-DI: 036074505901; Serial Numbers: CP86010393 DB68093186 CP87010814 CP86070669 CP86090743 CP86090744

Distribution pattern: US Nationwide distribution in the states of IL, MA, MN, NE, TX, and WI.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    bug in this firmware