Randox Laboratories Ltd.: Medical Device Recall in 2023 - (Recall #: Z-0199-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041, (2) RX4041R (refurbished)

Product Classification:

Class II

Date Initiated: September 6, 2023

Date Posted: November 8, 2023

Recall Number: Z-0199-2024

Event ID: 93102

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 6 units

Code Information:

GTIN: 05055273207781 Lot/Batch: (1) 7241-0616 7241-0582 7241-0441 7241-0425 7241-0384 RX4041R: Lot Number: (2) 7241-0149

Distribution Pattern:

US Nationwide distribution including Puerto Rico

Voluntary or Mandated:

Voluntary: Firm initiated