FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3893940 · Received June 12, 2014

Report

Report Number
3007981285-2014-01107
Event Type
Injury
Date Received
June 12, 2014
Date of Event
May 10, 2014
Report Date
May 15, 2014
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT RETURNING FOR EVAL. ATTEMPTS HAVE BEEN MADE TO OBTAIN ALL EVENT INFO. SHOULD NEW INFO BECOME AVAILABLE, A F/U MDR WILL BE SUBMITTED.

Description of Event or Problem · 1

RECEIVED INFO STATING CUSTOMER RECEIVED OCCLUSION ALARMS AND DEVELOPED DIABETIC KETOACIDOSIS. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
348651 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628

Patients

Seq Age Sex Outcome Treatment
1 16 YR Hospitalization