FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3940283 · Received June 19, 2014

Report

Report Number
3007981285-2014-01243
Event Type
Injury
Date Received
June 19, 2014
Date of Event
May 20, 2014
Report Date
May 20, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT RETURNING FOR EVALUATION. ATTEMPTS HAVE BEEN MADE TO OBTAIN ALL EVENT INFORMATION. SHOULD NEW INFORMATION BECOME AVAILABLE,A FOLLOW UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
360932 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 41 YR Other