FDA Adverse Event Malfunction Summary report: N

DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

MDR report key: 6716284 · Received July 14, 2017

Report

Report Number
3004753838-2017-42933
Event Type
Malfunction
Date Received
July 14, 2017
Date of Event
June 8, 2017
Report Date
June 21, 2017
Manufacturer
DEXCOM, INC.
Product Code
MDS
PMA / PMN Number
P120005
Removal / Correction Number
3004753838-02/29/16-001C
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

DEXCOM WAS MADE AWARE ON 06/21/2017 THAT ON (B)(6) 2017 THE RECEIVER HAD INTERMITTENT AUDIO OUTPUT. NO ADDITIONAL EVENT OR PATIENT INFORMATION IS AVAILABLE. NO PRODUCT OR DATA WAS PROVIDED FOR EVALUATION. THE REPORTED EVENT COULD NOT BE CONFIRMED. A ROOT CAUSE COULD NOT BE DETERMINED.

Description of Event or Problem · 1

THE COMPLAINT DEVICE WAS RETURNED FOR EVALUATION. THE DEVICE WAS VISUALLY INSPECTED AND NO DEFECTS WERE FOUND. THE RECEIVER WILL BOOT AND CHARGE. THE DOWNLOAD LOGS DOES NOT CONTAIN ANY ERRORS. RECEIVER PASSED ALL TESTS ON FUNCTIONAL TEST STATION EQ-900302-011.(PASSED AUDIO TEST). PASSED 'TRY IT','FIXED LOW' TEST AUDIO TONE WAS HEARD AT NORMAL VOLUME WHEN TESTED WITH RECEIVER COMMUNICATION TOOL : 7.0.0.75(LOW,MEDIUM,HIGH). OPENED RECEIVER, PASSED INTERNAL VISUAL INSPECTION. SPEAKER MEASURED 7.45 OHMS.(WITHIN TOLERANCE). PASSED 'WIGGLE' TEST. THE REPORTED EVENT OF AN INTERMITTENT AUDIO OUTPUT WAS NOT CONFIRMED. A ROOT CAUSE COULD NOT BE DETERMINED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
494575 DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM CONTINUOUS GLUCOSE MONITOR MDS DEXCOM, INC. MT20649-1 5223119

Patients

Seq Age Sex Outcome Treatment
1 7 YR