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Recall Observatory FDA recall evidence

Device product

The 4Kscore Test is an in vitro serum or plasma test that combines the results of four immunoassays (Roche Elecsys total PSA (prostate specific antigen), Roche Elecsys free PSA, intact PSA, and human kallikrein 2) into a single numerical score that also incorporates the following information: a patients age, previous biopsy, and digital rectal exam (DRE). Patients file (sample type, prior biopsy status, DRE status and age) are uploaded to the Specimen Processing Module (SPM). The results from the four assays are exported automatically to Lab Manager Application (B2 LIS) which automatically triggers the 4Kscore calculation when values of the four analytes are available. The 4Kscore test results are determined automatically by the validated laboratory information system algorithm calculation software.

Z-1676-2023

November 18, 2022

Class II

Product summary

Firm
BioReference Health, LLC
Event
Event 92205
Status
Ongoing
Classification
Class II
Quantity
1 system (662 Patients test results affected)
Official record key
device-enforcement:Z-1676-2023

Official wording

Reason: SPM software anomalies that may lead to the generation of erroneous 4Kscore Test results

Code information: UDI: 00850038860004

Distribution pattern: US Nationwide distribution in the state of New Jersey.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software anomalies