---
title: "StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683. ... — FDA record Z-0682-2025 | Is It on Recall"
description: "A software bug within the meter firmware leads to transmission of erroneous glucose and/or ketone patient test results to a healthcare institution's data manage"
url: https://isitonrecall.com/recall/fda-device-z-0682-2025-statstrip-glucose-ketone-hospital-meter-system-model-catalog-number-63683-prescription-use-blood-glu/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683. Prescription use blood glucose ketone me... — FDA record Z-0682-2025

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 Nov 20, 2024. 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**: StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683. Prescription use blood glucose ketone meter for near-patient testing
- **Reason**: A software bug within the meter firmware leads to transmission of erroneous glucose and/or ketone patient test results to a healthcare institution's data management system (DMS) at healthcare sites using WiFi if a user navigates to the Review Results screen while the meter is in the process of transmitting the current test result to the DMS.
- **Classification**: Class I
- **Recalling firm**: Nova Biomedical Corporation
- **Quantity**: 347 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0682-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0682-2025%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 | Model No 63683. UDI-DI (01)38548063685. Software versions: v0.0.13.10 to v0.0.13.44. |

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

## Distribution

Distribution US Nationwide including Puerto Rico, Germany, Italy, Israel, Switzerland, Australia, Great Britain, and the Netherlands.

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**: Jan 1, 2025
- **Recall initiation date**: Nov 20, 2024
- **Center classification date**: Dec 20, 2024

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-0682-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Nova Biomedical Corporation records](https://isitonrecall.com/brand/nova-biomedical-corporation/)
