FDA Adverse Event Malfunction Summary report: N

8100 ALARIS PUMP MODULE

MDR report key: 10916710 · Received November 29, 2020

Report

Report Number
2016493-2020-51142
Event Type
Malfunction
Date Received
November 29, 2020
Report Date
November 26, 2018
Manufacturer
CAREFUSION SD
Product Code
FRN
PMA / PMN Number
K133532
Removal / Correction Number
Z-1360-2020
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 TSC TROUBLESHOOTING PROCESS. A REVIEW OF THE DEVICE SERVICE HISTORY RECORD WAS PERFORMED FROM THE DATE OF MANUFACTURE TO THE DATE CORRESPONDING TO THIS SERVICE NOTIFICATION NUMBER. THE DATABASE SHOWED QUALITY NOTIFICATION WAS OPENED FOR THE DEVICE WITHOUT CORRELATION TO THE REPORTED COMPLAINT. 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 INVOLVED IN A PRODUCTION FAILURE, AND PRODUCT WAS RETURNED FOR SERVICING WHICH CORRELATES TO THE CUSTOMER REPORTED ISSUE. A REVIEW OF THE COMPLAINT HISTORY RECORD IN THE TRACKWISE WAS PERFORMED FOR THE SN (B)(4) WHICH CONFIRMED NO SIMILAR COMPLAINTS WITH THE SAME OR RELATED FAILURE MODE. THE CUSTOMER STATED THAT THERE WAS NO PATIENT INVOLVEMENT.

Description of Event or Problem · 1

(B)(4). 8100 13-1033-149 ERROR. SOFTWARE ERROR. UNIT CAME DOWN TO BIOMED WITH A NOTE SAYING 13-1033-149 ERROR. BIOMED COULD NOT DUPLICATE THE ERROR. RECOMMEND TO DO A PM AND RUN THE UNIT FOR AN HOUR TO SEE IF ANY ERROR COMES UP. IF SOFTWARE ERROR COMES UP, TRY TO REFLASH SOFTWARE AND IF FAILS REPLACE LOGIC BOARD. BIOMED WILL DO A PM AND RUN UNIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1381628 8100 ALARIS PUMP MODULE PUMP, INFUSION FRN CAREFUSION SD 8100

Patients

Seq Age Sex Outcome Treatment
1