Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172247 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G | 2 | 06/08/2023 |
FEI # 1018233 C.R. Bard Inc |
| Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF... | 2 | 06/08/2023 |
FEI # 1018233 C.R. Bard Inc |
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