DFI Co., Ltd.: 7 recalls on record
Recalls filed with 1 agency: FDA (7).
First recall on record: May 13, 2026. Most recent: May 13, 2026.
Risk classification: Class II: 7
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| May 13, 2026 | FDA | One Step UTI in vitro diagnostic test REF: 3374Z-2083-2026 | Z-2083-2026 |
| May 13, 2026 | FDA | One Step pH in vitro diagnostic test REF: 31I4PZ-2084-2026 | Z-2084-2026 |
| May 13, 2026 | FDA | QUCARE Total Cholesterol in vitro diagnostic test REF: 6407Z-2085-2026 | Z-2085-2026 |
| May 13, 2026 | FDA | One Step K in vitro diagnostic test REF: 81A4Z-2087-2026 | Z-2087-2026 |
| May 13, 2026 | FDA | One Step 10A in vitro diagnostic testZ-2082-2026 | Z-2082-2026 |
| May 13, 2026 | FDA | Uric Acid in vitro diagnostic test REF: 31H0PZ-2086-2026 | Z-2086-2026 |
| May 13, 2026 | FDA | One Step P in vitro diagnostic test REF: 8194Z-2088-2026 | Z-2088-2026 |
Questions about this company
- How many recalls does DFI Co., Ltd. have?
- Recalert has 7 U.S. recalls on record for DFI Co., Ltd., published between May 13, 2026 and May 13, 2026.
- What was the most recent DFI Co., Ltd. recall?
- FDA recall Z-2083-2026, published May 13, 2026: One Step UTI in vitro diagnostic test REF: 3374
- Which agencies have handled DFI Co., Ltd. recalls?
- DFI Co., Ltd. appears as the recalling firm in recalls from: FDA (7).
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