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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K150345
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FDA Recall
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HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 718... 2 06/08/2023 C.R. Bard Inc
Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF... 2 06/08/2023 C.R. Bard Inc
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