medical Class II Updated 2020-03-04

Randox Laboratories, Limited recalls RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (

Recalled Product

RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.


Hazard / Issue

Software version UI2550642107 for the RX Daytona + instrument released to correct the following issues: 1) The order of samples displayed is not sequential according to SID (sample identification number) when searching the run/results screen; 2) Incorrect color flagging of IQC as "out of range."

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Software version UI2550642107 for the RX Daytona Plus instrument.
View official government recall

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