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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K090901
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Product Description
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Recall
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FDA Recall
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EQUISTREAM® XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F 2 06/03/2020 Bard Peripheral Vascular Inc
EQUISTREAM® XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F 2 06/03/2020 Bard Peripheral Vascular Inc
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