Dexcom, Inc.: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 Us Retail Sensor/transmitter 1-pack Model/catalog Number: Stp-at...
Dexcom G7 Recall Summary Dexcom G7 glucose monitoring sensors from two specific lots were stolen during a destruction process and subsequently sold to pharmacies and distributors without authorization. One lot (1725204004) was being destroyed because the sensors were not properly sterilized and carry increased infection risk; the other lot (1725069002) was being destroyed due to risks of no sensor readings, inaccurate readings, or missed detection of high blood sugar events. These sensors were distributed across the United States and multiple other countries, and users may have already activated them through the Dexcom app.
- Recalling firm
- Dexcom, Inc.
- Product
- Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack Model/Catalog Number: STP-AT-012 Software Version: N/A Product Description: Dexcom G7 US Retail Sensor/Transmitter 1-pack Component: Dexcom G7 Continuous Glucose Monitoring System
- Reason
- Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and distributors by Pharmsource, LLC. Lot 1725204004 were designated for destruction because the G7 sensors were not properly sterilized and have an increased risk of skin infection if used. Lot 1725069002 were designated for destruction due to an increased risk of having no sensor readings available or experiencing sensor inaccuracy that includes the potential for missed detection of a hyperglycemic event or...
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-05-27
- Status
- Ongoing
- Distribution
- Dexcom does not have distribution records for this product due to its unauthorized release. However Dexcom is able to identify sensor session starts for the affected lots through the Dexcom G7 CGM App user performance data. Based on App user performance data, Lot 1725204004 has sensor session...
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/3881b7ef-00d0-408d-89a5-0058ca68255f