FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4840206 · Received June 11, 2015

Report

Report Number
3007981285-2015-33716
Event Type
Injury
Date Received
June 11, 2015
Date of Event
May 12, 2015
Report Date
May 12, 2015
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS EXPECTED TO BE RETURNED; HOWEVER, THE DEVICE HAS NOT YET BEEN RECEIVED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PUMP STOPPED ALL INSULIN DELIVERY. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED (427 MG/DL). IT WAS CONFIRMED THAT THE CUSTOMER HAD ALTERNATE INSULIN THERAPY AVAILABLE AND WOULD TAKE A CORRECTION SHOT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
382716 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 18 YR Other