FDA Adverse Event Malfunction Summary report: N

G4 PLATINUM PEDIATRICS CONTINUOUS GLUCOSE MONITORING SYSTEM

MDR report key: 3900821 · Received June 27, 2014

Report

Report Number
3004753838-2014-04857
Event Type
Malfunction
Date Received
June 27, 2014
Date of Event
June 3, 2014
Report Date
June 3, 2014
Manufacturer
DEXCOM, INC.
Product Code
MDS
PMA / PMN Number
P120005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Additional Manufacturer Narrative · 1

(B)(4). EVALUATION OF THE RETURNED DEVICE DID NOT CONFIRM THE REPORTED INTERMITTENT AUDIO OUTPUT.

Description of Event or Problem · 1

PATIENT'S MOTHER CONTACTED DEXCOM TECHNICAL SUPPORT ON (B)(6) 2014 TO CLAIM NO AUDIO OUTPUT ON (B)(6) 2014. AT THE TIME OF THE CALL TO DEXCOM TECHNICAL SUPPORT, NO MEDICAL INTERVENTION OR INJURIES WERE REPORTED. ADDITIONALLY, DURING THE CALL, DEXCOM TECHNICAL SUPPORT ADVISED PATIENT'S MOTHER TO TEST THE ALERT FUNCTIONALITY AND PATIENT'S MOTHER REPORTED ALERTS WERE FUNCTIONAL. DEXCOM HAS ISSUED AN RGA FOR PATIENT'S MOTHER TO RETURN THE DEVICE TO BE INVESTIGATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
377338 G4 PLATINUM PEDIATRICS CONTINUOUS GLUCOSE MONITORING SYSTEM MDS MDS DEXCOM, INC. MT22430 5135363

Patients

Seq Age Sex Outcome Treatment
1 4 YR Other