FDA Adverse Event Malfunction Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 5163597 · Received October 21, 2015

Report

Report Number
3007981285-2015-56049
Event Type
Malfunction
Date Received
October 21, 2015
Date of Event
September 30, 2015
Report Date
September 30, 2015
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS EXPECTED TO BE RETURNED; HOWEVER, THE DEVICE HAS NOT YET BEEN RECEIVED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED. DEVICE NOT RETURNED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A MALFUNCTION ALARM OCCURRED AND THE PUMP STOPPED ALL INSULIN DELIVERY. THERE WAS NO REPORTED IMPACT TO THE CUSTOMER'S BLOOD GLUCOSE LEVEL. IT WAS CONFIRMED THAT THE CUSTOMER WOULD USE AN ALTERNATE INSULIN THERAPY TO ENSURE THAT INSULIN DELIVERY IS NOT INTERRUPTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
695287 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG 004628

Patients

Seq Age Sex Outcome Treatment
1 64 YR