FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3954571 · Received July 18, 2014

Report

Report Number
3007981285-2014-03126
Event Type
Injury
Date Received
July 18, 2014
Date of Event
June 21, 2014
Report Date
June 22, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RECEIVED FOR EVALUATION. HOWEVER, THE EVALUATION IS NOT COMPLETE. A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF EVALUATION.

Description of Event or Problem · 1

RECEIVED INFORMATION STATING CUSTOMER'S PUMP UNEXPECTEDLY RESET. PER CUSTOMER, BLOOD GLUCOSE LEVEL WENT UP TO 300.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
423146 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 66 YR Other