Class II

Medical Device Recall: Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)

Visgeneer, Inc. · October 4, 2023

Reason for Recall

Due to products distributed without premarket clearance or approvals.

Distribution

Worldwide - U.S. Nationwide distribution in the states of CA and MI. The country of Canada.

States Affected

NATIONWIDE

Quantity Affected

2580

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2501-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.