FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3961550 · Received June 16, 2014

Report

Report Number
3007981285-2014-03234
Event Type
Injury
Date Received
June 16, 2014
Date of Event
June 18, 2014
Report Date
June 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
FL, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT RETURNING FOR EVALUATION. SHOULD NEW INFORMATION BECOME AVAILABLE, A FOLLOW UP REPORT WILL BE SUBMITTED. USE OF APIDRA INSULIN IS CONTRAINDICATED FOR THE T:SLIM CARTRIDGE.

Description of Event or Problem · 1

RECEIVED INFORMATION STATING CUSTOMER RECEIVED MULTIPLE OCCLUSION ALARMS. REPORTEDLY CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED. CUSTOMER WAS USING APIDRA INSULIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
351969 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 29 YR Other INSULIN: APIDRA