Drug recall
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
FDA recall event 82351 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 82351 |
|---|---|
| Recall numbers | Z-0252-2020 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage. |
| Initiation date | Mar 7, 2019 |
| Report date | Nov 6, 2019 |
| Termination date | Feb 11, 2022 |
| 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: