FDA Adverse Event Malfunction Summary report: N

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

MDR report key: 3841865 · Received May 30, 2014

Report

Report Number
3004753838-2014-08368
Event Type
Malfunction
Date Received
May 30, 2014
Date of Event
May 4, 2014
Report Date
May 4, 2014
Manufacturer
DEXCOM, INC.
Product Code
MDS
PMA / PMN Number
P120005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PATIENT CONTACTED DEXCOM TECHNICAL SUPPORT ON (B)(6) 2014 TO REPORT CGM INACCURACIES COMPARED TO BLOOD GLUCOSE METER ON (B)(6) 2014. DEXCOM REVIEWED RECEIVER DATA ON (B)(6) 2014. DATA CONFIRMED SOME READINGS WERE OUTSIDE OF THE 20 PERCENT/20 POINT DIFFERENCE RANGE AT THE TIME OF THE CALL TO DEXCOM TECHNICAL SUPPORT, THE PATIENT DID NOT REPORT ANY MEDICAL INTERVENTION OR INJURIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
319667 G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM MDS MDS DEXCOM, INC. 9500-27 5131300

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other