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Meridian Bioscience Inc Recalls

12 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Meridian Bioscience Inc.

12Total Recalls
0Critical
6,562Units Affected
Dec 5, 2025Most Recent
All Recalls

Every Meridian Bioscience Inc Recall

Sorted by most recent. Click any recall for full details.

12 recalls
High RiskFDA
Meridian Bioscience Inc
Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300
Diagnostic Devices·211 affected·Dec 5, 2025
High RiskFDA
Meridian Bioscience Inc
Meridian Bioscience, alethia c. Difficile, Catalog Number 480050, Nucleic Acid Amplification Test Assay
Diagnostic Devices·109 affected·Oct 7, 2025
High RiskFDA
Meridian Bioscience Inc
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay
Diagnostic Devices·109 affected·Oct 7, 2025
High RiskFDA
Meridian Bioscience Inc
Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens co...
Medical Devices·38 affected·Oct 19, 2023
High RiskFDA
Meridian Bioscience Inc
Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal ...
Medical Devices·201 affected·Oct 19, 2023
High RiskFDA
Meridian Bioscience Inc
Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog Number: 410700
Medical Devices·92 affected·Dec 15, 2022
High RiskFDA
Meridian Bioscience Inc
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog N...
Diagnostic Devices·452 affected·Feb 15, 2022
High RiskFDA
Meridian Bioscience Inc
Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative t...
Medical Devices·376 affected·Apr 8, 2021
High RiskFDA
Meridian Bioscience Inc
The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of ...
Medical Devices·8 affected·Feb 8, 2021
High RiskFDA
Meridian Bioscience Inc
PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay (EIA) is a sc...
Diagnostic Devices·184 affected·Dec 17, 2018
High RiskFDA
Meridian Bioscience Inc
PREMIER EHEC and PREMIER EHEC Bulk.
Medical Devices·4,747 affected·Nov 8, 2016
High RiskFDA
Meridian Bioscience Inc
illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with illumigene Mole...
Diagnostic Devices·35 affected·Apr 22, 2014