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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1017-2025
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Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated... 2 01/23/2025 FEI # 1000361607
Randox Laboratories, Limited
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