FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3812692 · Received May 5, 2014

Report

Report Number
3007981285-2014-00560
Event Type
Injury
Date Received
May 5, 2014
Date of Event
April 8, 2014
Report Date
April 9, 2014
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RECEIVED FOR EVALUATION; HOWEVER, DEVICE EVALUATION IS NOT YET COMPLETE. A FOLLOW UP MDR WILL BE FILED.

Description of Event or Problem · 1

RECEIVED INFORMATION REGARDING MULTIPLE CARTRIDGE ALARMS (CARTRIDGE ALARM 19) DURING THE LOAD PROCESS. THE REPORTED ISSUE IMPACTED CUSTOMER'S BLOOD GLUCOSE LEVEL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
267864 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628

Patients

Seq Age Sex Outcome Treatment
1 25 YR Other