Device recall
Z-2007-2019: 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
FDA device recall · Class II · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-2007-2019 |
|---|---|
| Recall event | 82138 |
| Product | 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573 |
| Product code | FMF |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2020 |
| 510(k) numbers | K980987 |
| FEI number | 2243072 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database