---
title: "The 4Kscore Test, an in vitro serum or plasma test that combines the results ... — FDA record Z-0516-2024 | Is It on Recall"
description: "Mathematical modeling of the 4Kscore with and without DRE information was recently performed on over 3,000 specimens. DRE information is a required component of"
url: https://isitonrecall.com/recall/fda-device-z-0516-2024-the-4kscore-test-an-in-vitro-serum-or-plasma-test-that-combines-the-results-of-four-immunoassays-roc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# The 4Kscore Test, an in vitro serum or plasma test that combines the results of four immunoassays (Roche Elecsys tota... — FDA record Z-0516-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 31, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: The 4Kscore Test, 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 patient s age, previous biopsy, and digital rectal exam (DRE).
- **Reason**: Mathematical modeling of the 4Kscore with and without DRE information was recently performed on over 3,000 specimens. DRE information is a required component of The 4Kscore Test.
- **Classification**: Class II
- **Recalling firm**: BioReference Health, LLC
- **Quantity**: 1 system (3,196 tests)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0516-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0516-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00850038860004 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Dec 20, 2023
- **Recall initiation date**: Oct 31, 2023
- **Center classification date**: Dec 8, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0516-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [BioReference Health, LLC records](https://isitonrecall.com/brand/bioreference-health-llc/)
