FDA Adverse Event Malfunction Summary report: N

ALARIS SYSTEM

MDR report key: 17440614 · Received August 2, 2023

Report

Report Number
2016493-2023-205092
Event Type
Malfunction
Date Received
August 2, 2023
Date of Event
July 10, 2023
Report Date
September 12, 2023
Manufacturer
CAREFUSION SD
Product Code
FRN
UDI-DI
10885403811012
PMA / PMN Number
K133532
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

A DEVICE HISTORY RECORD REVIEW IS PERFORMED ON EACH DEVICE REPORTED IN A MDR REPORTABLE EVENT ALONG WITH OTHER METHODS OF INVESTIGATION AS CODED IN SECTION H6 OF THIS MDR REPORT. PER 803.52(F)(11)(III) THE INFORMATION PROVIDED WAS OBTAINED FROM SERVICING ACTIVITIES PERFORMED ON THE DEVICE. THERE WERE NO ADDITIONAL DETAILS OBTAINABLE OR PROVIDED AT THE TIME OF SERVICE. SEE MANUFACTURER NARRATIVE.

Additional Manufacturer Narrative · 0

CORRECTION: UNIQUE IDENTIFIER (UDI) #. ANNEX B: B21. ANNEX C: C21. ANNEX D: D16. ADDITIONAL INFORMATION: DEVICE AVAILABLE FOR EVAL?, RETURNED TO MANUFACTURER ON, DEVICE RETURN TO MANUF .?, DEVICE EVAL BY MANUFACTURER? ANNEX A: A040507, A070903, A0721, A0401. ANNEX G: G02005, G0201204, G04061. ANNEX B: B01. ANNEX C: C02, C07. ANNEX D: D02, D15.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE DEVICE HAD ALARMS FOR NO APPARENT REASON AND CALIBRATION ERROR. THERE WAS NO PATIENT INVOLVEMENT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE DEVICE HAD ALARMS FOR NO APPARENT REASON AND CALIBRATION ERROR. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1157982 ALARIS SYSTEM PUMP, INFUSION FRN CAREFUSION SD 8110 10885403811012

Patients

Seq Age Sex Outcome Treatment
1 Unknown