Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product… — Class II medical device recall Z-2574-2026
Ongoing recall by Dexcom, Inc., reported 2026-07-01. Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen duri
| Recall number | Z-2574-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dexcom, Inc., San Diego, CA, United States |
| Recall initiated | 2026-05-27 |
| Classified | 2026-06-24 |
| Reported by FDA | 2026-07-01 |
| Countries outside the US | AE, AT, AU, CA, CH, CZ, DE, ES, FI, FR, GB, HK, IL, IT, JP, KR, KW, NL, PL, PT, QA, SG, TR |
| UPC / GTIN / UDI-DI | 00386270004109 |
| Lot numbers | 1725069002, 1725204004 |
| Model numbers | STP-AT-012 |
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 for recall
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 incorrect treatment decisions that can result in patient injury, including medical intervention to prevent permanent injury or impairment. Additionally, due to the unknown storage and handling and storage conditions these sensors may have undergone during the distribution, these sensors may present additional risk.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2574-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.