FDA Adverse Event Malfunction Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3950739 · Received June 9, 2014

Report

Report Number
3007981285-2014-01029
Event Type
Malfunction
Date Received
June 9, 2014
Date of Event
May 9, 2014
Report Date
May 9, 2014
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RECEIVED FOR EVALUATION; HOWEVER, DEVICE EVALUATION IS NOT YET COMPLETE. A FOLLOW-UP MDR WILL BE FILED.

Description of Event or Problem · 1

RECEIVED INFORMATION REGARDING A CARTRIDGE ALARM 1 DURING BOLUS DELIVERY. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS NOT IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
334989 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628 M002472

Patients

Seq Age Sex Outcome Treatment
1 25 YR