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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K240902
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Recall
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FDA Recall
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Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor... 2 06/24/2026 FEI # 3004753838
Dexcom, Inc.
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App ... 2 05/11/2026 FEI # 3004753838
Dexcom, Inc.
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Mod... 2 05/11/2026 FEI # 3004753838
Dexcom, Inc.
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