Device recall
Z-0207-2018: BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These…
FDA device recall · Class II · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-0207-2018 |
|---|---|
| Recall event | 77639 |
| Product | 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 insulin injection. |
| Product code | FMI |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2018 |
| 510(k) numbers | K021475 |
| 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