Medical DeviceSep 10, 2025
Visgeneer Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device recall — FDA Z-2501-2025
Due to products distributed without premarket clearance or approvals.
Class IIFDA: OngoingVisgeneer, Inc.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceSep 10, 2025
Visgeneer Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device recall — FDA Z-2500-2025
Due to products distributed without premarket clearance or approvals.
Class IIFDA: OngoingVisgeneer, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Visgeneer, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.