PlainRecalls

Randox Laboratories, Limited

13 recalls on record · Latest: Jan 29, 2025

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Agency notice ledger

Federal filing book Randox Laboratories, Limited LIGHT-BOOK · SINGLE-AGENCY

#1,200 of 14,151 · 13 notices · 0.012% archive

  • BOOK 13 notices
  • RANK #1,200 of 14,151
  • SHARE 0.012% archive
  • AGENCY FDA Devices (13)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 29, 2025
  • PHOTO Access Scientific LLC

Nearest notice-volume peer: Access Scientific LLC (0 notice gap)

Randox Laboratories, Limited accounts for about 0.012% of the 104,423-notice archive on 13 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Randox Laboratories, Limited sits among 14,151 recalling firms

Randox Laboratories, Limited ranks 1,200th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Randox Laboratories, Limited vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

13 1200th of 14151 higher than 12,927 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Randox Laboratories, Limited in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Randox Laboratories, Limited holds about 0.012% of archive notices alongside 13 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 29, 2025

Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP2757

FDA Devices Moderate Jan 29, 2025

Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP3403

FDA Devices Moderate Mar 4, 2020

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.

FDA Devices Moderate Nov 27, 2019

Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.

FDA Devices Moderate Nov 27, 2019

Randox Liquid Cardiac Controls Catalogue Number CQ5051

FDA Devices Moderate Nov 27, 2019

Randox Liquid Cardiac Controls Catalogue Number CQ5052.

FDA Devices Low Nov 20, 2019

RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.

FDA Devices Moderate Aug 14, 2019

Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Human Assayed Multi-sera is for the control of accuracy.

FDA Devices Low Aug 14, 2019

Assayed Bovine Multi-Sera Level 1, Model No. AL1027

FDA Devices Moderate Jul 31, 2019

RX Daytona, Model Nos. RX4040 and RX4041

FDA Devices Moderate Jul 31, 2019

RX Imola, Model Nos. RX4900

FDA Devices Moderate Mar 21, 2018

Liquid Cardiac Control CQ5053

FDA Devices Moderate Dec 14, 2016

Magnesium on RX Imola analyser IVD

Randox Laboratories, Limited holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (13 here — thin-book).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Randox Laboratories, Limited?
PlainRecalls indexes 13 distinct federal recall events naming Randox Laboratories, Limited, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Randox Laboratories, Limited sit among other recalling firms?
Randox Laboratories, Limited ranks #1,200 of 14,151 by distinct recall-event count among 14,151 firms in this archive (91st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Randox Laboratories, Limited's notices?
FDA Devices accounts for 13 of this firm's 13 indexed notices.
What product category dominates Randox Laboratories, Limited's filing book?
Filings for Randox Laboratories, Limited span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Randox Laboratories, Limited: 13 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Randox Laboratories, Limited; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026