FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4151970 · Received October 6, 2014

Report

Report Number
3007981285-2014-09313
Event Type
Injury
Date Received
October 6, 2014
Date of Event
September 12, 2014
Report Date
September 12, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE PRODUCT HAS NOT BEEN RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED

Description of Event or Problem · 1

CUSTOMER INQUIRED ABOUT THE PURPOSE OF THE INCOMPLETE TEMP ALERT RATE AS CUSTOMER'S BLOOD GLUCOSE LEVEL WAS SLIGHTLY LOW. TANDEM TECHNICAL SUPPORT ADDRESSED CUSTOMER'S INQUIRY AND CUSTOMER WAS SATISFIED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
623867 TANDEM T:SLIM INSULIN DELIVERY SYSTEM LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 8 YR Other