FDA Adverse Event Injury Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3934605 · Received June 27, 2014

Report

Report Number
3007981285-2014-01639
Event Type
Injury
Date Received
June 27, 2014
Date of Event
May 28, 2014
Report Date
May 28, 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
GA, 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 MDR WILL BE SUBMITTED.

Description of Event or Problem · 1

RECEIVED INFORMATION STATING CUSTOMER RECEIVED NOTIFICATION THAT SITE REQUIRED CHANGING. CUSTOMER BELIEVES THIS NOTIFICATION WAS RECEIVED IN ERROR. REPORTEDLY, CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
375944 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 55 YR Other