FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3842683 · Received May 19, 2014

Report

Report Number
3007981285-2014-00683
Event Type
Injury
Date Received
May 19, 2014
Date of Event
April 20, 2014
Report Date
April 21, 2014
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN REC'D FOR EVALUATION; HOWEVER, DEVICE EVALUATION IS NOT YET COMPLETE. A F/U MDR WILL BE FILED.

Description of Event or Problem · 1

REC'D INFO REGARDING A CARTRIDGE ALARM 1 DURING BASAL DELIVERY. REPORTEDLY, IT IS UNKNOWN IF THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
295143 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628 M003380

Patients

Seq Age Sex Outcome Treatment
1 33 YR Other