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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Recalling Firm
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Z-0186-2024 - Alaris PCA Module 8120 1 11/07/2023 CareFusion 303, Inc.
Z-0184-2024 - BD Alaris PCU REF 8015 1 11/07/2023 CareFusion 303, Inc.
Z-0185-2024 - BD Alaris Syringe Module, REF 8110 1 11/07/2023 CareFusion 303, Inc.
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