ClearanceBrief
Recall Z-2083-2019 ยท JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

Randox Laboratories, Limited

RX Daytona, Model Nos. RX4040 and RX4041

DateJun 24, 2019
StatusTerminated
ReasonThere was a report of a malfunction with the sensor which resulted in an increase of temperature leading to melting of internal wires and scorch damage to the internal structure of the instrument.
Root causeUnder Investigation by firm
ActionOn June 24, 2019, the firm notified its customers of the recall through an Urgent Field Safety Notice. Customers were asked to take the following actions: If there is any sign of damage to the RCU lid or lid sensor " Switch of main analyser main power supply as soon as possible " Contact technical support immediately. " Discuss the contents of this notice with your Medical Director. " Display this notice in a prominent location near the instrument. " Complete and return the response form 12187-QA to technical.services@randox.com within five working days.
Quantity3
DistributionDomestic distribution to CA CT MA MD MO NC NJ NY OH PA UT WV and PR. Worldwide foreign distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K131554RX DAYTONA PLUS CHEMISTRY ANALYZER; RX DAYTONA PLUS ASPARTATE AMINOTRANSFERASE (AST) REAGENT
Randox Laboratories, Ltd., Jan 9, 2014