FDA Adverse Event Malfunction Summary report: N

CADD

MDR report key: 11668224 · Received April 14, 2021

Report

Report Number
3012307300-2021-03143
Event Type
Malfunction
Date Received
April 14, 2021
Report Date
February 21, 2022
Manufacturer
ST PAUL
Product Code
FPA
UDI-DI
10610586027239
PMA / PMN Number
K040636
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

OTHER, OTHER TEXT: H6: EVENT PROBLEM AND EVALUATION CODES: UPDATED AFTER DEVICE EVALUATION. H10: DEVICE EVALUATION: THE DEVICES WERE RETURNED FOR INVESTIGATION. SAMPLES RECEIVED: THE SAMPLES CONSIST OF TWENTY-FOUR (24) CASSETTE UNITS FROM P/N 21-7302-24 L/N 4092490; THE RETURNED SAMPLES WERE RECEIVED IN NEW CONDITION WITH ITS ORIGINAL CLOSED PACKAGE. VISUAL INSPECTION: THE SAMPLES WERE VISUALLY INSPECTED AT A DISTANCE OF 12" TO 16" UNDER NORMAL CONDITIONS OF ILLUMINATION TO DETECT SAMPLES CONDITIONS THAT COULD CAUSE FUNCTIONAL ISSUES. RESULTS: THE SAMPLES DIDN?T PRESENT ANY DAMAGE, SCUFFS, PINCH MARKS, CRACKS, CRAZING, ETC. COULD CAUSE THE FAILURE MODE REPORTED. FUNCTIONAL TESTING: SAMPLES WERE FILLED WITH WATER; THE SAMPLES WERE CONNECTED TO THE CADD LEGACY PLUS TO LOOK FOR UNUSUAL FUNCTION. RESULTS: THE SAMPLES WERE FULLY PRIMING AND CONNECTED WITHOUT DIFFICULT, THE PUMP WERE SET RUNNING AND THE ALARM WERE NOT ACTIVATED. THE COMPLAINT WAS NOT CONFIRMED. NO ACTIONS TAKEN WERE PERFORMED SINCE THE COMPLAINT WAS NOT CONFIRMED.

Description of Event or Problem · 1

INFORMATION WAS RECEIVED REGARDING A CADD CASSETTE RESERVOIR. IT WAS REPORTED THAT PATIENT INVOLVED RECEIVED AN ERROR MESSAGE STATING, "NO DISPOSABLE PUMP- WON'T RUN." THE MESSAGE WAS RECEIVED ANYWHERE FROM 2 HOURS AFTER INFUSION BEGAN TO 12 HOURS AFTER. THE PUMP WAS USED THE DAY BEFORE WITH NO ERROR MESSAGES. AFTER TROUBLESHOOTING, THE PUMP INFUSED SUCCESSFULLY FOR 10 MINUTES WITH A DIFFERENT CASSETTE FROM A DIFFERENT LOT. THERE WERE THREE PATIENTS INVOLVED IN THIS INCIDENT. AS A RESULT, SOME PATIENTS WERE UNABLE TO GET CHEMO THERAPY FOR SEVERAL HOURS. THEY HAD TO GO TO THE EMERGENCY ROOM. NO INJURIES WERE NOTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
564611 CADD INTRAVASCULAR ADMINISTRATION SET FPA ST PAUL 21-7302-24 4092490 10610586027239

Patients

Seq Age Sex Outcome Treatment
1 Unknown