Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K241078 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion p... | 1 | 11/05/2025 | Tandem Diabetes Care, Inc. |
| t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071,... | 2 | 10/23/2025 | Tandem Diabetes Care, Inc. |
| Tandem Mobi Insulin Pump with Interoperable Technology | 1 | 04/11/2025 | Tandem Diabetes Care, Inc. |
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