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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0976-2025 - BD Pyxis Med 4000 Auxiliary (AUX), REF 314 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
Z-0975-2025 - BD Pyxis Med ES Auxiliary (AUX), REF 343 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
Z-0974-2025 - BD Pyxis MedStation 4000 AUX, REF 306 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
Z-0973-2025 - BD Pyxis MedStation 4000 Main, REF 303 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
Z-0971-2025 - BD Pyxis MedStation ES (Med ES Main), REF 323 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
Z-0972-2025 - BD Pyxis MedStation ES AUX, REF 324 2 01/17/2025 FEI # 2016493
CareFusion 303, Inc.
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