FDA Adverse Event Injury Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4100779 · Received September 12, 2014

Report

Report Number
3007981285-2014-08039
Event Type
Injury
Date Received
September 12, 2014
Date of Event
September 1, 2014
Report Date
September 1, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
111210
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NE, US
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 HAD HIGH BLOOD GLUCOSE LEVELS (276 MG/DL). CUSTOMER CHANGED HIS CARTRIDGE AND INFUSION SET TO STABILIZE HIS BLOOD GLUCOSE LEVELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
565123 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628 M003858

Patients

Seq Age Sex Outcome Treatment
1 14 YR Other