Drug recall
BD Vacutainer Specimen Collection Cups, Cat. No. 364975
FDA recall event 81148 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 81148 |
|---|---|
| Recall numbers | Z-0491-2019, Z-0492-2019, Z-0493-2019, Z-0494-2019 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Vacutainer Specimen Collection Cups, Cat. No. 364975, BD Vacutainer Urine Collection Cups, Cat. No. 364941, KIT URIN CUP 16X100 8.0 CONI UA YEL, Cat. No. 364989 BD Vacutainer Urine Cup Kit with UA Tube for Midstream Specimens, KIT URIN CUP PLC 16X100 10.0 UA YEL, Cat. No. 364981: Urine Collection Kit for collection and transport of urine specimens for urinalysis |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical Practice… |
| Initiation date | Aug 30, 2018 |
| Report date | Nov 28, 2018 |
| Termination date | Oct 21, 2020 |
| City | Franklin Lakes |
| State | NJ |
| Country | United States |
| FEI number | 2243072 |
At a glance
- 1–9 Products in this recall
- 10–99 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: