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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
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Z-1698-2023 - Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818 2 06/08/2023 C.R. Bard Inc
Z-1701-2023 - HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818 2 06/08/2023 C.R. Bard Inc
Z-1700-2023 - Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G 2 06/08/2023 C.R. Bard Inc
Z-1699-2023 - Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 53810G, g) REF 53812G, h) REF 53814G, i) REF 53816G, j... 2 06/08/2023 C.R. Bard Inc
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