FDA Adverse Event Malfunction Summary report: N

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

MDR report key: 3760138 · Received April 18, 2014

Report

Report Number
3004753838-2014-07468
Event Type
Malfunction
Date Received
April 18, 2014
Date of Event
March 21, 2014
Report Date
March 21, 2014
Manufacturer
DEXCOM, INC.
Product Code
MDS
PMA / PMN Number
P120005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PATIENT CONTACTED DEXCOM TECHNICAL SUPPORT ON (B)(6) 2014 TO REPORT CGM INACCURACY COMPARED TO BLOOD GLUCOSE METER ON (B)(6) 2014. AT THE TIME OF THE CALL TO DEXCOM TECHNICAL SUPPORT, PATIENT DID NOT REPORT ANY MEDICAL INTERVENTION OR INJURIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
237191 G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM MDS MDS DEXCOM, INC. 9500-27 5090173

Patients

Seq Age Sex Outcome Treatment
1 60 YR Other