DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
Report
- Report Number
- 3004753838-2019-041856
- Event Type
- Malfunction
- Date Received
- May 14, 2019
- Date of Event
- April 17, 2019
- Report Date
- May 16, 2019
- Manufacturer
- DEXCOM, INC.
- Product Code
- PQF
- UDI-DI
- 00386270000613
- PMA / PMN Number
- P120005
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). THE PATIENT EXPERIENCED ADVERSE EVENTS ON DIFFERENT DAYS WITH THE SAME DEVICE. THE FOLLOWING REPORTS ARE BEING SUBMITTED: 190418-003481,190418-003602,190418-003622,190418-003632,190418-003644,190418-003660,190418-003673,190418-003682,190418-003701,190418-003719 ,190418-003586.
(B)(4).
IT WAS REPORTED THAT A LOSS OF CONNECTION OCCURRED. A REVIEW OF THE SHARE LOGS WAS PERFORMED AND A LOSS OF CONNECTION WAS FOUND WITHIN THE INVESTIGATION WINDOW. HOWEVER, THE DEVICE OPERATED WITHIN SPECIFICATION. THE ALLEGATION WAS NOT CONFIRMED. THE PROBABLE CAUSE COULD NOT BE DETERMINED. NO INJURY OR MEDICAL INTERVENTION WAS REPORTED.
IT WAS REPORTED THAT A LOSS OF CONNECTION OCCURRED.THE PRODUCT WAS EVALUATED. AN EXTERNAL VISUAL INSPECTION WAS PERFORMED AND PASSED. RECEIVER CHARGES AND BOOT UP: PASSED. PERFORM PARING\CALIBRATION\PERFORMANCE\RANGE TEST: PASSED. TEST ON RECEIVER FUNCTIONAL TEST STATION: PASSED ALL RELEVANT TESTING. DOWNLOAD RX LOG AND PERFORM REVIEW OF THE RX LOG AND A LOSS OF CONNECTION WAS FOUND WITHIN THE INVESTIGATION WINDOW. THE ALLEGATION WAS CONFIRMED. THE PROBABLE CAUSE COULD NOT BE DETERMINED. NO INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 401513 | DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM | CONTINUOUS GLUCOSE MONITOR | PQF | DEXCOM, INC. | MT22719 | 5252258 | 00386270000613 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 80 YR |