FDA recall Z-2083-2019

Randox Laboratories, Limited · Class II · device

Product

RX Daytona, Model Nos. RX4040 and RX4041

Reason for recall

There 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.

Distribution

Domestic distribution to CA CT MA MD MO NC NJ NY OH PA UT WV and PR. Worldwide foreign distribution.

Key facts

Status
Terminated
Initiation date
2019-06-24
Report date
2019-07-31
Termination date
2020-05-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Crumlin, N/A, United Kingdom

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2083-2019