DFI Co., Ltd. recalls

7 recalls on record · latest: April 2, 2026

Official U.S. recall history for DFI Co., Ltd., compiled from official government records.

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DFI Co., Ltd. recalls One Step UTI in vitro diagnostic test REF: 3374

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step 10A in vitro diagnostic test

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step pH in vitro diagnostic test REF: 31I4P

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step P in vitro diagnostic test REF: 8194

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls Uric Acid in vitro diagnostic test REF: 31H0P

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step K in vitro diagnostic test REF: 81A4

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…