FDA Adverse Event Malfunction Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4152433 · Received October 6, 2014

Report

Report Number
3007981285-2014-08864
Event Type
Malfunction
Date Received
October 6, 2014
Date of Event
September 10, 2014
Report Date
September 12, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NE, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

FOLLOW UP SAME DAY INDICATED THAT CUSTOMER DECLINED FURTHER TROUBLESHOOTING AND BLOOD GLUCOSE LEVEL WAS "DOING WELL". 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

IT WAS REPORTED THAT THE CUSTOMER RECEIVED MULTIPLE OCCLUSION ALARMS. THERE WAS NO REPORTED IMPACT TO CUSTOMER'S BLOOD GLUCOSE LEVEL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
622282 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 35 YR INSULIN: HUMALOG| INFUSION SET: INSET