PlainRecalls

Randox Laboratories

Compiled from official public sources by the publisher.

6 recalls on record · Latest: Apr 5, 2023

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Agency notice ledger

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

#2,268 of 14,151 · 6 notices · 0.006% archive

  • BOOK 6 notices
  • RANK #2,268 of 14,151
  • SHARE 0.006% archive
  • AGENCY FDA Devices (6)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 5, 2023
  • PHOTO 1908 Brands

Nearest notice-volume peer: 1908 Brands (0 notice gap)

Randox Laboratories accounts for about 0.006% of the 104,423-notice archive on 6 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 sits among 14,151 recalling firms

Randox Laboratories ranks 2,268th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Randox Laboratories vs all firms by recall-notice count

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

6 2268th of 14151 higher than 11,804 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 in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Randox Laboratories holds about 0.006% of archive notices alongside 6 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 5, 2023

CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of CRP concentration in serum Catalogue number: CP3826
FDA Devices Moderate Jun 13, 2018

RX Imola (RX4900) For Professional Use for the quantitative in vitro determination of various clinical chemistry tests.
FDA Devices Low Mar 21, 2018

Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)
FDA Devices Low Mar 21, 2018

Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)
FDA Devices Low Jun 7, 2017

Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In-Vitro Diagnostic Urinary Clinical Assays on a range of clinical chemistry systems.
FDA Devices Moderate Dec 21, 2016

The Randox Liquid Cardiac Controls Level 1, Level 2, and Level 3 are liquid controls containing BNP, CK MB Mass, Digoxin, D-Dimer, Homocysteine, hsCRP, Myoglobin, NT-ProBNP, Troponin I, and Troponin T. They have been developed for use in the quality control of BNP, CK MB Mass, Digoxin, D-Dimer, Homocysteine, hsCRP, Myoglobin, NT-ProBNP, Troponin I, and Troponin T assays on various clinical chemistry and immunoassay systems. This in vitro diagnostic device is intended for prescription use only.

Randox Laboratories 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 (6 here).

1908 Brands 6 Abbott Molecular 6 Accriva Diagnostics, Inc. 6 Advance Medical Designs, Inc. 6 Agave Dream 6

Similar medical devices volume

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

Abbott Molecular 6 Accriva Diagnostics, Inc. 6 Advance Medical Designs, Inc. 6 American Medical Systems, Inc. 6

Frequently Asked Questions

How many federal recall notices name Randox Laboratories? ▼
PlainRecalls indexes 6 distinct federal recall events naming Randox Laboratories, 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 sit among other recalling firms? ▼
Randox Laboratories ranks #2,268 of 14,151 by distinct recall-event count among 14,151 firms in this archive (83rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Randox Laboratories's notices? ▼
FDA Devices accounts for 6 of this firm's 6 indexed notices.
What product category dominates Randox Laboratories's filing book? ▼
Filings for Randox Laboratories 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: 6 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; individual notices remain authoritative on each linked recall page.

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