FDA Adverse Event Injury Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3850415 · Received May 15, 2014

Report

Report Number
3007981285-2014-00634
Event Type
Injury
Date Received
May 15, 2014
Date of Event
April 15, 2014
Report Date
April 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 WERE MADE TO OBTAIN ALL AVAILABLE INFO. SHOULD NEW INFO BECOME AVAILABLE, A F/U MDR WILL BE SUBMITTED.

Description of Event or Problem · 1

RECEIVED INFO STATING CUSTOMER RECEIVED AN OCCLUSION ALARM. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
291553 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES 004628 M002334

Patients

Seq Age Sex Outcome Treatment
1 38 YR Other INSULIN SET: INSET| INSULIN: NOVOLOG