FDA Adverse Event Injury Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3893740 · Received June 4, 2014

Report

Report Number
3007981285-2014-00960
Event Type
Injury
Date Received
June 4, 2014
Date of Event
May 6, 2014
Report Date
May 6, 2014
Manufacturer
TANDEM DIABETES
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RECEIVED FOR EVAL; HOWEVER, DEVICE EVAL IS NOT YET COMPLETE. A FOLLOW UP MDR WILL BE FILED.

Description of Event or Problem · 1

RECEIVED INFO REGARDING A CARTRIDGE ALARM 19 DURING BASAL DELIVERY. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
327280 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other