Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K251032 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) | 2 | 04/02/2026 |
FEI # 3003166194 Medtronic MiniMed, Inc. |
| MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The Mi... | 2 | 02/02/2026 |
FEI # 3003166194 Medtronic MiniMed, Inc. |
| MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61 | 2 | 03/24/2026 |
FEI # 3003166194 Medtronic MiniMed, Inc. |
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