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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-1748-2025
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Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time rev... 2 05/12/2025 FEI # 3005248192
Abbott Molecular, Inc.
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