FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3950965 · Received July 14, 2014

Report

Report Number
3007981285-2014-03121
Event Type
Injury
Date Received
July 14, 2014
Date of Event
June 13, 2014
Report Date
June 13, 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

NO PRODUCT RETURNING FOR EVAL. SHOULD NEW INFO BECOME AVAILABLE, A SUPPLEMENTAL FORM WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER EXPERIENCED HIGH BLOOD GLUCOSE LEVELS. CUSTOMER USED INJECTION TO CORRECT HIGH BLOOD GLUCOSE. CUSTOMER ON MENSES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
410326 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628 M002680

Patients

Seq Age Sex Outcome Treatment
1 13 YR Other