Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K232380 |
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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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| t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim mobile app) | 2 | 09/24/2025 |
FEI # 3007981285 Tandem Diabetes Care, Inc. |
| t:slim X2 Insulin Pump with Interoperable Technology | 1 | 04/11/2025 |
FEI # 3007981285 Tandem Diabetes Care, Inc. |
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