FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP

MDR report key: 7342671 · Received March 15, 2018

Report

Report Number
3013756811-2018-08311
Event Type
Malfunction
Date Received
March 15, 2018
Date of Event
November 15, 2017
Report Date
March 15, 2018
Manufacturer
TANDEM DIABETES CARE
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT WAS RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT MULTIPLE INTERMITTENT OCCLUSION ALARMS OCCURRED. BLOOD GLUCOSE RANGED FROM 140-350 MG/DL. REPORTEDLY, THE SUPPLIES WERE CHANGED TO ADDRESS THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
184366 T:SLIM X2 INSULIN PUMP INSULIN PUMP LZG TANDEM DIABETES CARE 1000096

Patients

Seq Age Sex Outcome Treatment
1 41 YR INFUSION SET: TRUSTEEL, INSULIN: CONTACT DETACH