Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K211575 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-5... | 1 | 06/30/2026 |
FEI # 3014585508 Insulet Corporation |
| Omnipod (Eros) Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 (10 Pack), POD- ZXP420 (... | 1 | 06/30/2026 |
FEI # 3014585508 Insulet Corporation |
| 18239: ASM Omnipod Dash PDM, insulin delivery system. PT-000010: Assembly, Dash Final PDM U100, m... | 1 | 11/15/2022 |
FEI # 3014585508 Insulet Corporation |
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