Meridian Bioscience, Inc.
11 devices · 15 adverse event reports · 1 deaths reported · 7 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Revogene 610210Real Time Nucleic Acid Amplification System2 recalls10 reports
- Para-Pak Zn-PVA / 10% Formalin 301012Fixative, Metallic Containing1 recall0 reports
- ImmunoCard Mycoplasma 709030Enzyme Linked Immunoabsorbent Assay, Mycoplasma Spp.1 recall0 reports
- Para-Pak CLEAN 900312Container, Specimen, Sterile1 recall0 reports
- Alethia™ C. difficile 480050C. Difficile Nucleic Acid Amplification Test Assay1 recall0 reports
- Alethia™ Group B Streptococcus 480350Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test1 recall0 reports
- Revogene C. difficile 410300C. Difficile Toxin Gene Amplification Assay1 recall0 reports
- BreathTek UBT for H. pylori 01Test, Urea Adult And Pediatric (Breath),2 reports
- illumigene Group B Streptococcus 280350Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test1 report
- ImmunoCard STAT! EHEC 751630Antigens, All Types, Escherichia Coli1 death1 report
- Alethia™ 610189Real Time Nucleic Acid Amplification System1 report