Remel, Inc.
16 devices · 1 adverse event reports · 15 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.
- REMEL R02041Culture Media, Selective And Differential3 recalls0 reports
- REMEL R01144Culture Media, Selective And Non-Differential1 recall0 reports
- REMEL R01202Culture Media, Non-Selective And Differential1 recall0 reports
- REMEL R01272Culture Media, Selective And Non-Differential1 recall0 reports
- NA R01460Culture Media, For Isolation Of Pathogenic Neisseria1 recall0 reports
- NA R01503Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar1 recall0 reports
- Strep Selective II Agar R01859Culture Media, Selective And Differential1 recall0 reports
- REMEL R02049Culture Media, Selective And Differential1 recall0 reports
- NA R04030Culture Media, For Isolation Of Pathogenic Neisseria1 recall0 reports
- NA R04033Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar1 recall0 reports
- REMEL R064810Culture Media, Selective Broth1 recall0 reports
- NA Y3462Susceptibility Test Plate, Antifungal1 recall0 reports
- NA CP112-10Manual Antimicrobial Susceptibility Test Systems1 recall0 reports
- NA CP114-10Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth1 recall0 reports
- Sensititre Supplemental Brucella Broth T3450Culture Media, General Nutrient Broth1 recall0 reports
- NA R01186Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar1 report