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Recall Observatory FDA recall evidence

Device product

StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog Number: 63910. Prescription use blood glucose ketone meter for near-patient testing

Z-0683-2025

November 20, 2024

Class I

Product summary

Firm
Nova Biomedical Corporation
Event
Event 95783
Status
Ongoing
Classification
Class I
Quantity
1,615 units
Official record key
device-enforcement:Z-0683-2025

Official wording

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.

Code information: Model No 63910. UDI-DI (01)1038548063910. Software Versions: v0.0.13.10 to v0.0.13.44.

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

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software bug