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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Dexcom, Inc. Dexcom G6 Continuous Glucose Monitoring System

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Dexcom, Inc. Dexcom G6 Continuous Glucose Monitoring System Back to Search Results
Model Number 9445-02
Medical Device Problem Code Wireless Communication Problem (3283)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/05/2026
Type of Reportable Event Malfunction
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Brand Name
Dexcom G6 Continuous Glucose Monitoring System
Common Device Name
Continuous Glucose Monitor
Manufacturer (Section D)
Dexcom, Inc.
6340 sequence dr.
san diego CA 92121
Manufacturer (Section G)
Dexcom, Inc.
6340 sequence dr.
san diego CA 92121
Manufacturer Contact
jaime chavez
6340 sequence dr.
san diego, CA 92121
+1(858)200-0200
MDR Report Key50509626
Report Number3004753838-2026-239379
Device Sequence Number9209913
Product Code QBJ
UDI-Device Identifier00386270000385
UDI-Public(01)00386270000385(11)190118(10)5246640
Combination Product (Y/N)N
Initial Reporter StateNC
Initial Reporter CountryUS
PMA/510(K) Number
DEN170088
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Consumer
Type of Report Initial
Report Date (Section B) 08/28/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Lay User/Patient
Device Model Number9445-02
Device Catalogue NumberSTT-OE-001
Device Lot Number5246640
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Received by Manufacturer 08/05/2026
Initial Report FDA Received Date08/28/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured01/18/2019
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient Age41 YR
Patient SexMale
Patient Weight185 LB
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