Greiner Bio-One North America recalls
Greiner Bio-One North America has 16 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 26 Nov 2025. 4 are still ongoing. 2 were reported in the last 12 months.
Total recalls16since 2012
Last 12 months2reported
Class I00% of total
Ongoing4latest 26 Nov 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 16 100%Class III 0 0%
Why greiner bio-one north america is recalled
Product types
By year
Ongoing greiner bio-one north america recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Vacuette CAT Serum Separator Clot Activator recalled | Greiner Bio-One North America | Potency & Assay | 28 states |
| Device | CLASS II | Greiner Bio-one Vacuette 9NC Coagulation sodium citrate recalled | Greiner Bio-One North America | Other | Nationwide |
| Device | CLASS II | Vacuette¿ Tube Cat Serum Separator Clot Activator red recalled | Greiner Bio-One North America | Device Malfunction | Nationwide |
| Device | CLASS II | Vacuette Tube FX Sodium Fluoride/Potassium Oxalate recalled | Greiner Bio-One North America | Lead & Heavy Metals | Nationwide |
All greiner bio-one north america recalls, newest first
16 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.