⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Is Dfi recalled?

Dfi recalls - full list & free alerts

Official U.S. agency records list 7 recalls involving Dfi in the last 12 months, most recently on 2026-05-13. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (7)

DFI Co., Ltd.: One Step 10A in vitro diagnostic test
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: One Step UTI in vitro diagnostic test REF: 3374
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: One Step pH in vitro diagnostic test REF: 31I4P
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: QUCARE Total Cholesterol in vitro diagnostic test REF: 6407
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: Uric Acid in vitro diagnostic test REF: 31H0P
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: One Step K in vitro diagnostic test REF: 81A4
Medical DevicesFDA (device) · 2026-05-13 · Class II
DFI Co., Ltd.: One Step P in vitro diagnostic test REF: 8194
Medical DevicesFDA (device) · 2026-05-13 · Class II
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