Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K223931 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and G6 Pro Andro... | 1 | 10/30/2025 | Dexcom, Inc. |
| Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1) | 1 | 06/16/2025 | Dexcom, Inc. |
| Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OR-001 | 2 | 02/20/2025 | Dexcom, Inc. |
| Dexcom G6, Continuous Glucose Monitoring System, REFs: STK-OM-001, STR-OM-001, STR-OR-001 | 2 | 02/20/2025 | Dexcom, Inc. |
| Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OE-001 | 2 | 02/20/2025 | Dexcom, Inc. |
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