Drug recall
VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.
FDA recall event 85215 · Class II · Greiner Bio-One North America, Inc.
Key facts
| Event ID | 85215 |
|---|---|
| Recall numbers | Z-1714-2020 |
| Recalling firm | Greiner Bio-One North America, Inc. |
| Product type | Devices |
| Products | VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate. |
| Initiation date | Mar 12, 2020 |
| Report date | Apr 22, 2020 |
| Termination date | Aug 31, 2022 |
| City | Monroe |
| State | NC |
| Country | United States |
| FEI number | 3001451379 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: