FDA Enforcement Class II Ongoing

RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number: RX4040

Recall: Z-0198-2024 · Reported November 8, 2023

Enforcement

Recall Number
Z-0198-2024
Event ID
93102
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Randox Laboratories Ltd.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 8, 2023
Initiation Date
September 6, 2023
Classification Date
October 31, 2023
Address
55 Diamond Road, N/A, Crumlin (North), N/A, N/A, Ireland

Description

RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number: RX4040

Reason

RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly.

Code Info

GTIN: 05055273207774 Lot/ Batch Number (1) Lot/ Batch Number 7241-0551 7241-0545 7241-0531 7241-0317 7241-0219

Distribution

US Nationwide distribution including Puerto Rico

Quantity

5 units