FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4132832 · Received September 29, 2014

Report

Report Number
3007981285-2014-08322
Event Type
Injury
Date Received
September 29, 2014
Date of Event
September 3, 2014
Report Date
September 3, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
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

RECEIVED INFORMATION THAT CUSTOMER HAD CHANGED CARBOHYDRATE USING THINKING THAT IT WOULD CHANGE THE BOLUS SETTING. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED. CUSTOMER SUCCESSFULLY RESET SETTINGS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
606467 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 61 YR Other