Drug recall
BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general…
FDA recall event 77639 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 77639 |
|---|---|
| Recall numbers | Z-0207-2018 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Hub damage resulting in breakage and/or leakage during use. |
| Initiation date | May 31, 2017 |
| Report date | Dec 13, 2017 |
| Termination date | Jun 28, 2018 |
| 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: