FDA Adverse Event Malfunction Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3905214 · Received May 29, 2014

Report

Report Number
3007981285-2014-00863
Event Type
Malfunction
Date Received
May 29, 2014
Date of Event
April 30, 2014
Report Date
April 30, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

CUSTOMER DID NOT WANT TO TROUBLESOOT HIGH BG'S AS SHE KNEW THAT SHE HAD FORGOTTEN TO BOLUS AND BELIEVED THAT WAS THE CAUSE.

Description of Event or Problem · 1

RECEIVED INFORMATION STATING PATIENT WAS EXPERIENCING HIGH BG'S (335 MG/DL) AS SHE HAD FORGOTTEN TO BOLUS EARLIER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
317393 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 19 YR