Uric Acid in vitro diagnostic test REF: 31H0P - The devices were distributed without required FDA premarket clearance or approval.

Source: FDA | Recall date: 05/13/2026

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Affected product: Uric Acid in vitro diagnostic test REF: 31H0P

Summary: The devices were distributed without required FDA premarket clearance or approval.

Hazard: The devices were distributed without required FDA premarket clearance or approval.

Track your baby products and get automatic recall alerts when something may affect your family.