Class IIOngoingZ-2086-2026
DFI Co., Ltd. recalls Uric Acid in vitro diagnostic test REF: 31H0P
The devices were distributed without required FDA premarket clearance or approval.
DFI Co., Ltd.May 13, 2026
Acid, Uric, Uricase (Colorimetric) recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–1 of 1 recalls