Meridian Bioscience Inc
12 recalls on record · Latest: Jan 14, 2026
FDA Devices Moderate Jan 14, 2026
Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300
FDA Devices Moderate Nov 26, 2025
Meridian Bioscience, alethia c. Difficile, Catalog Number 480050, Nucleic Acid Amplification Test Assay
FDA Devices Moderate Nov 26, 2025
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay
FDA Devices Moderate Dec 20, 2023
Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens containing int…
FDA Devices Moderate Dec 20, 2023
Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites C…
FDA Devices Moderate Feb 1, 2023
Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog Number: 410700
FDA Devices Moderate Apr 6, 2022
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210…
FDA Devices Moderate May 19, 2021
Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative test run on t…
FDA Devices Moderate Mar 31, 2021
The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of recent Mycop…
FDA Devices Moderate Jan 23, 2019
PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay (EIA) is a screening or a…
FDA Devices Moderate Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
FDA Devices Moderate Jul 9, 2014