FDA Adverse Event Malfunction Summary report: N

MEDSYTEM III INFUSION PUMP

MDR report key: 11299987 · Received February 9, 2021

Report

Report Number
2016493-2021-25057
Event Type
Malfunction
Date Received
February 9, 2021
Report Date
October 22, 2018
Manufacturer
CAREFUSION SD
Product Code
FRN
UDI-DI
10885403928659
PMA / PMN Number
K933545
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

THIS REPORTED EVENT AND SUBSEQUENT REPAIRS WERE INVESTIGATED THROUGH THE SERVICE REPAIR PROCESS. FAILURE DATA AND PARTS-USED INFORMATION WERE REVIEWED FOR THE SAP AND TRACK WISE FILES AND FOUND RELEVANT TO THE SERVICE REPAIR. A REVIEW OF THE SOURCE DEVICE SERVICE HISTORY RECORD WAS PERFORMED FROM THE DATE OF MANUFACTURE TO THE DATE CORRESPONDING TO THIS SERVICE NOTIFICATION NUMBER. THE DATABASE SHOWED NO QUALITY NOTIFICATIONS WERE OPENED FOR THE DEVICE. A REVIEW OF THE DEVICE HISTORY RECORD IN SAP FOR SN (B)(4) WAS PERFORMED FROM THE DATE OF THE MANUFACTURE TO DATE OF THE RELEASE OF PRODUCT, WHICH CONFIRMED THAT THIS DEVICE WAS NOT INVOLVED IN A PRODUCTION FAILURE, AND PRODUCT WAS RETURNED FOR SERVICING WHICH CORRELATES TO THE CUSTOMER REPORTED ISSUE. A TRACKWISE COMPLAINT HISTORY REVIEW WAS COMPLETED, AND IT WAS CONFIRMED THAT THERE WERE ADDITIONAL COMPLAINTS RECEIVED WITH SIMILAR SN (B)(4) FOR THE SAME OR RELATED FAILURE MODE. THE CUSTOMER STATED THAT THERE WAS NO PATIENT INVOLVEMENT.

Description of Event or Problem · 1

CHANNEL A CARTRIDGE JAM & SERVICE 10/22/2018 06:36:13 ZENITH SOMANI (ZSOMANI) PHONE 800-387-8309 1 THERE IS NO PATIENT INVOLVEMENT. 11/09/2018 07:46:38 SENTHURAN SIVASAMBO (SSIVASAM) 1ZR236E61443135478

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
200876 MEDSYTEM III INFUSION PUMP PUMP, INFUSION FRN CAREFUSION SD 2865 10885403928659

Patients

Seq Age Sex Outcome Treatment
1