Drug recall
BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product…
FDA recall event 83507 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 83507 |
|---|---|
| Recall numbers | Z-0193-2020 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Separation of front and rear barrels upon activation of the safety feature that retracts the needle |
| Initiation date | Jul 31, 2019 |
| Report date | Oct 30, 2019 |
| Termination date | Jul 27, 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: