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Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland Recalls

All product recalls associated with Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 641–660 of 4099 recalls

RX Series Urea Enzymatic Assay (Randox) – Carryover Bias (2023)

Carryover from the Direct LDL-cholesterol assay on the Rx instruments may result in a negative bias, up to -11%, in quality control and patient samples, in urea assays results if the urea assay is run immediately after the Direct LDL-cholesterol assay. This may lead to a delay in reporting results or in falsely decreased urea test results.

FDAJun 13, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Bronchovideoscope BF Type (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

EVIS EXERA III Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

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FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

EVIS EXERA Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Bronchofiberscope BF Type (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

HF Resection Electrodes (Olympus) – Wire Breakage Caution (2023)

Additional Caution statements in IFU: (1) Due to complaints where the loop wire at the distal end of the HF resection electrode broke after getting in contact with metal objects, such as other endoscopic equipment, implants or stents. As a result, fragments can fall inside the patient and must be retrieved. (2) The second Caution refers to the risk of sparkover when getting in contact with metal parts as this can cause uncontrolled heating of the HF-resection electrode and may result in damage and breakage to the HF-resection electrode tip

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

OES Bronchofiberscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

EVIS EXERA II Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Narskido Infant Bath Seats (TopGlore) – drowning risk (2023)

This recall involves Narskido infant bath seats. The molded plastic bath seats are light blue and white and have suction cups at the bottom, a removable handle at the front and a temperature card at the back of the base.

CPSCJun 8, 2023Nationwide• Yiwu Jingtong Maternal and Infant Products Co. Ltd., of China

NanoZoomer S360MD Slide Scanner (Hamamatsu) – Incorrect Barcode Identification (2023)

If the wrong barcode information is recorded in the NDPi file, a pathologist may refer to the whole slide image (WSI) of a different patient.

FDAJun 6, 2023NY• Hamamatsu Corporation

Fanta Orange 12pk (Coca-Cola) – Incorrect sugar labeling (2023)

Immediate package labeled as zero sugar contains the full sugar variety

Class IIModerate

FDAJun 1, 2023CA• Great Lakes Coca-Cola Distribution LLC

UFSK Treatment Chair 500 XLE (UFSK) – Drive Mechanism Wear (2023)

Service life of the electrical seat part drive of the treatment chair may be shortened unexpectedly after several years of use due to a potential wear-related reduction in the self-locking of the drive and may remain undetected. A worsened self-locking of the seat drive can lead to overriding the drive s end position when positioning the patient with the seat part in an inclined position

FDAMay 31, 2023Nationwide• UFSK International OSYS Gmbh Kirchhoffstr. 1 Ratisbon Germany

Bugatti Chiron Super Sport (BUGATTI) – Incorrect Wheel Installation (2023)

Bugatti (Bugatti) is recalling one 2023 Chiron Super Sport vehicle. The incorrect wheels were installed on the vehicle.

NHTSAMay 31, 2023Nationwide• BUGATTI

Prima TT Genoid Baseplate (Limacorporate) – Hole Specification Issue (2023)

Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.

FDAMay 30, 2023Nationwide• Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy

Prima TT Genoid Monoblock Baseplate (Limacorporate) – Hole Specification Issue (2023)

Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.

FDAMay 30, 2023Nationwide• Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy

VISERA Tracheal Intubation Videoscope (Olympus) – Reprocessing Compatibility (2023)

Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs. The addendum highlights the following changes: 1. Removal of LF-V and LF-P as compatible with the OER 2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO 3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes remain compatible

FDAMay 26, 2023Nationwide• Olympus Corporation of the Americas

Tracheal Intubation Fiberscope (Olympus) – Reprocessing Compatibility (2023)

Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs. The addendum highlights the following changes: 1. Removal of LF-V and LF-P as compatible with the OER 2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO 3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes remain compatible

FDAMay 26, 2023Nationwide• Olympus Corporation of the Americas

Olympus Endoscope Reprocessor (Olympus) – Reprocessing Compatibility (2023)

Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs. The addendum highlights the following changes: 1. Removal of LF-V and LF-P as compatible with the OER 2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO 3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes remain compatible

FDAMay 26, 2023Nationwide• Olympus Corporation of the Americas

EliA GBM Wells, Material Number 14551401, for Phadia 250,... (Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden) – complaints that specific samples prod... (2023)

Complaints that specific samples produced false positive EliA GBM results. A positive signal was present when these samples were tested for coating-solution reactivity using EliA wells without antigen.

FDAMay 24, 2023Nationwide• Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden