FDA Adverse Event Injury Summary report: N

TANDEM T:SLM INSULIN DELIVERY SYSTEM

MDR report key: 3003865 · Received March 12, 2013

Report

Report Number
3007981285-2013-00012
Event Type
Injury
Date Received
March 12, 2013
Date of Event
February 11, 2013
Report Date
February 12, 2013
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

EVENT NOT LIKELY TO LEAD TO SERIOUS INJURY OR DEATH, T:SLIM USER GUIDE INSTRUCTS USERS TO "ROUTINELY CHECK THEIR BG LEVELS AT LEAST 4 TIMES DAILY (OPTIMALLY 6 - 8 TIMES DAILY) IN ORDER TO DETECT HYPERGLYCEMIA AND HYPOGLYCEMIA EARLY." ADDITIONALLY, T:SLIM USER GUIDE CAUTIONS USERS "TO PREVENT DKA OR A VERY HIGH BG, YOU MUST BE PREPARED TO INJECT INSULIN IF DELIVERY IS INTERRUPTED FOR ANY REASON." IT IS COMMON PRACTICE FOR INSULIN USERS TO CHECK BLOOD GLUCOSE VALUES FREQUENTLY TO PREVENT LEVELS FROM BECOMING SEVERE ENOUGH TO CAUSE SERIOUS COMPLICATIONS.

Description of Event or Problem · 1

SCHOOL NURSE REPORTED HER STUDENT WAS EXPERIENCING HIGH BLOOD GLUCOSE LEVELS. THE NURSE ADMINISTERED INSULIN WHICH BROUGHT THE LEVELS DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
103481 TANDEM T:SLM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628

Patients

Seq Age Sex Outcome Treatment
1 14 YR