DFI Co., Ltd.

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-05-13 to 2026-05-13

Date	Source	Product	Brand	Severity	Units
2026-05-13	FDA Device	FDA Recall: One Step K in vitro diagnostic test REF: 81A4	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: Uric Acid in vitro diagnostic test REF: 31H0P	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: QUCARE Total Cholesterol in vitro diagnostic test REF: 6407	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: One Step P in vitro diagnostic test REF: 8194	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: One Step pH in vitro diagnostic test REF: 31I4P	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: One Step UTI in vitro diagnostic test REF: 3374	DFI Co., Ltd.	Class II	N/A
2026-05-13	FDA Device	FDA Recall: One Step 10A in vitro diagnostic test	DFI Co., Ltd.	Class II	N/A