Device recall
Z-2889-2020: BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
FDA device recall · Class II · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-2889-2020 |
|---|---|
| Recall event | 86120 |
| Product | BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack |
| Product code | FMI |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2021 |
| 510(k) numbers | K951254 |
| 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