---
title: "STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vit... — FDA record Z-0490-2024 | Is It on Recall"
description: "Deterioration in the stability of the Test Strips results in diminished low-range detection capability and inability to meet linearity performance claims. The r"
url: https://isitonrecall.com/recall/fda-device-z-0490-2024-stat-site-m-bhb-test-strips-used-with-stat-site-m-beta-hb-meter-as-an-in-vitro-diagnostic-for-blood/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values. — FDA record Z-0490-2024

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 2, 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**: STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.
- **Reason**: Deterioration in the stability of the Test Strips results in diminished low-range detection capability and inability to meet linearity performance claims. The root cause of the stability deterioration in is identified as the change in material that caused a pH shift in the coating solution resulting in precipitation during coating runs. The device defect can cause false negative results that may lead to a delay in treatment of patients with associated conditions such as diabetic ketoacidosis.
- **Classification**: Class II
- **Recalling firm**: Stanbio Laboratory, LP
- **Quantity**: 2,351
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0490-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0490-2024%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: 00657498000090, Lot/Expiration: 203044/2024-01-31, 209644/2024-06-30 |

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

## Distribution

Worldwide - US Nationwide distribution including in the states of AZ, RI, MO, UT, AK, LA, TX, OH, GA, MN, NY, CA, NJ, IL, WA, KS, MI, NC, PA, MA, CO, KY, NM, FL, MD, VA, IN, AL, SD, MS, WV, WI, ID, MT, WY and the countries of Canada and Singapore.

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

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## Dates in the source

- **Report date**: Dec 13, 2023
- **Recall initiation date**: Oct 2, 2023
- **Center classification date**: Dec 6, 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-0490-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stanbio Laboratory, LP records](https://isitonrecall.com/brand/stanbio-laboratory-lp/)
