FDA Adverse Event Injury Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4337756 · Received December 15, 2014

Report

Report Number
3007981285-2014-15379
Event Type
Injury
Date Received
December 15, 2014
Date of Event
November 18, 2014
Report Date
November 18, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL LOT NUMBER WERE REPORTED: LOT# M002695 AND LOT# UNK; HOWEVER, THE CAUSE OF THE EVENT IS NOT DUE TO THE CARTRIDGES. THE DEVICE HAS BEEN RECEIVED FOR EVAL; HOWEVER, DEVICE EVAL IS NOT YET COMPLETE. A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE EVAL.

Description of Event or Problem · 1

RECEIVED INFO REGARDING MULTIPLE CARTRIDGE ALARMS (CARTRIDGE ALARM 19) WITH MULTIPLE CARTRIDGES DURING THE LOAD PROCESS. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
820588 TANDEM T:SLIM INSULIN DELIVERY SYSTEM LZG TANDEM DIABETES CARE INC. 004628 M001822

Patients

Seq Age Sex Outcome Treatment
1 19 YR Other