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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2082-2026 - One Step 10A in vitro diagnostic test 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2083-2026 - One Step UTI in vitro diagnostic test REF: 3374 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2084-2026 - One Step pH in vitro diagnostic test REF: 31I4P 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2088-2026 - One Step P in vitro diagnostic test REF: 8194 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2086-2026 - Uric Acid in vitro diagnostic test REF: 31H0P 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2087-2026 - One Step K in vitro diagnostic test REF: 81A4 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
Z-2085-2026 - QUCARE Total Cholesterol in vitro diagnostic test REF: 6407 2 05/06/2026 FEI # 3005841640
DFI Co., Ltd.
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