Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K203768 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Omnipod 5 Automated Insulin Delivery System | 2 | 09/20/2023 | Insulet Corporation |
| Omnipod 5 Automated Insulin Delivery System Product catalog numbers: PT-000409: ASM, Omnipod 5, PD... | 2 | 12/07/2022 | Insulet Corporation |
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