Back to signals
FDA device recallVulnerabilitiesPublished September 11, 2026

Nova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient Testing

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also a

Open the source record
Tags
FDA recall, medical device, class 2, Clinical Chemistry, Software design, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 6: Security Assessment and Testing; CISSP 8: Software Development Security; CISM 3: Information Security Program
Source record id
Z-3132-2026
First seen by InfoSec Signals
9/23/2026

Exam domain labels come from a keyword heuristic and are study hints, not an official mapping. The summary is the publisher's own text, shortened; the linked record is authoritative.