FDA Adverse Event Malfunction Summary report: N

PICCOLO XPRESS

MDR report key: 5013321 · Received August 19, 2015

Report

Report Number
5013321
Event Type
Malfunction
Date Received
August 19, 2015
Date of Event
July 14, 2015
Report Date
August 3, 2015
Manufacturer
ABAXIS, INC
Product Code
JJG
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

EARLIER THIS SUMMER, THE INFUSION CENTER NURSING STAFF BEGAN TO NOTICE THAT POTASSIUM RESULTS THAT THEY WERE GETTING FROM THE PICCOLO POCT MACHINE WERE UNUSUALLY LOW. THEY SENT BLOOD SAMPLES TO THE HOSPITAL LAB AND DISCOVERED THERE WAS A LARGE DISCREPANCY IN THE RESULTS (>0.5). THE REPRESENTATIVE FROM ABAXIS WAS NOTIFIED AND A LOANER MACHINE WAS PROVIDED A WEEK LATER, WHILE THE MANUFACTURER INVESTIGATED THE MACHINE. ON TWO WEEKS AFTER THE ORIGINAL IDENTIFICATION OF THIS PROBLEM, THE STAFF AGAIN BEGAN TO NOTICE LOW POTASSIUM RESULTS ON THE LOANER MACHINE AND WHEN THE SAMPLES WERE SENT TO THE HOSPITAL LAB, THERE WAS AN UNACCEPTABLE DISCREPANCY. MULTIPLE LOT NUMBERS AND CONTROLS WERE DONE AND IT WAS NARROWED DOWN TO 3 LOT NUMBERS OF THE DISC THAT IS USED IN THE MACHINE. THE MANUFACTURER WAS NOTIFIED AND INDICATED THAT THERE WAS NOT A RECALL ON THE LOT NUMBERS IDENTIFIED BY STAFF. PRIOR TO THE LOANER MACHINE, THERE WERE 6-12 INCORRECT RESULTS IDENTIFIED. SINCE THE LOANER HAS BEEN IN USE, 13 ERRORS IN RESULTS HAS OCCURRED ON MULTIPLE PATIENTS. THERE HAS BEEN NO PATIENT HARM, ONE PATIENT DID RECEIVE 20 MCQ OF K+, HOWEVER, THERE WAS NO HARM. THE INFUSION CENTER NURSING STAFF CONTINUES TO CLOSELY MONITOR EVERY POTASSIUM RESULT. MANUFACTURER RESPONSE FOR PICCOLO XPRESS CHEMISTRY ANALYZER, (BRAND NOT PROVIDED) (PER SITE REPORTER). THE REPRESENTATIVE WAS CONTACTED AS WELL AS ABAXIS TECHNICAL SUPPORT. THE ORIGINAL MACHINE WAS RETURNED TO ABAXIS PER THEIR REQUEST SO THEY COULD INVESTIGATE AS INITIALLY IT WAS THOUGHT TO BE AN ERROR WITH THE MACHINE AND THAT PERHAPS THE MACHINE NEEDED CLEANING (PER ABAXIS). HOWEVER, AFTER THE LOANER MACHINE WAS RECEIVED (7/14/2015) 13 ADDITIONAL ERRORS WERE DISCOVERED. AFTER MULTIPLE LOT NUMBERS AND CONTROLS WERE TESTED, IT WAS NARROWED DOWN TO THE DISCS AND 3 DIFFERENT LOT NUMBERS. THE 3 LOT NUMBERS WERE RETURNED AND REPLACEMENTS OF DIFFERENT LOT NUMBERS WERE RECEIVED. WHEN ASKED SPECIFICALLY IF A RECALL WOULD TAKE PLACE, STAFF WERE TOLD NOT AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
547445 PICCOLO XPRESS ANALYZER, CHEMISTRY, CENTRIFUGAL, FOR CLINICAL USE JJG ABAXIS, INC 5225AB6,

Patients

Seq Age Sex Outcome Treatment
1