The FDA announced on July 29, 2026, that Nova Biomedical Corporation is recalling the StatStrip Glucose and B-Ketone meter (Model No. 63683) due to a software defect. The hazard involves incorrect patient data transmission resulting from barcode scanning errors.
How to tell if you have it
- Brand: Nova Biomedical
- Product: StatStrip Glucose and B-Ketone meter
- Model No: 63683
- UDI-DI: 00385480636834
- Software Versions: All versions 0.00.13.10 through 1.5.14.25
- Quantity: 1,858 units
The hazard
A software synchronization issue causes the device to intermittently retain previously scanned barcodes, leading to incorrect patient glucose results being assigned to medical records. This defect affects both patient identification and quality control barcode scanning but does not impact analytical accuracy. The FDA reported no specific incidents or injuries in this record.
Context
GovInfoNow's records show Nova Biomedical Corporation has 3 other recalls on record since June 19, 2017. Other recent recalls of similar products include Medtronic CareLink Clinic Software Error May Cause Incorrect Glucose Readings (Oct. 21, 2025), GE Medical Systems ECG Systems Software Error Risks Patient Data Mix-Up (April 21, 2026), and GE Healthcare Centricity Enterprise Archive V2/V3/V4 Software Recall: Patient Data Mismatch Risk (July 31, 2026).