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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEXCOM, INC. DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING SYSTEM

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DEXCOM, INC. DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING SYSTEM Back to Search Results
Model Number STS-OE-003
Device Problem Detachment of Device or Device Component (2907)
Patient Problems Foreign Body In Patient (2687); No Clinical Signs, Symptoms or Conditions (4582)
Event Date 11/07/2021
Event Type  malfunction  
Manufacturer Narrative
(b)(4).
 
Event Description
It was reported that detached sensor wire occurred.The sensor was inserted into the abdomen on (b)(6) 2021.No product was provided for evaluation.The allegation and a probable cause could not be determined.No injury or medical intervention was reported.
 
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Brand Name
DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING SYSTEM
Type of Device
CONTINUOUS GLUCOSE MONITOR
Manufacturer (Section D)
DEXCOM, INC.
6340 sequence dr
san diego CA 92121
Manufacturer Contact
ashley spoto
6340 sequence dr
san diego, CA 92121
8582000200
MDR Report Key12940768
MDR Text Key283145394
Report Number3004753838-2021-307442
Device Sequence Number1
Product Code QDK
Combination Product (y/n)Y
Reporter Country CodeUS
PMA/PMN Number
K182041
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Other
Type of Report Initial
Report Date 12/06/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/06/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Expiration Date10/31/2022
Device Model NumberSTS-OE-003
Device Catalogue NumberSTS-OE-003#S-P#00386270000866
Device Lot Number7290462
Was Device Available for Evaluation? No
Date Manufacturer Received11/07/2021
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured04/28/2021
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Age5 YR
Patient SexMale
Patient Weight19 KG
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