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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K190502
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Cardinal Health Monoject, 6ML Enteral Syringe (purple) Low Dose (LDT) - For Use with ENFit Connectio... 1 02/02/2024 Cardinal Health 200, LLC
Cardinal Health Monoject, 60mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF... 1 02/02/2024 Cardinal Health 200, LLC
Cardinal Health Monoject, 35mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF ... 1 02/02/2024 Cardinal Health 200, LLC
Cardinal Health Monoject, 12mL Enteral Syringe (purple) For Use with ENFit Connection System, REF 4... 1 02/02/2024 Cardinal Health 200, LLC
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