Device recall
Z-0022-2009: BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for…
FDA device recall · Class II · Becton Dickinson and Company
Key facts
| Recall number (Z-number) | Z-0022-2009 |
|---|---|
| Recall event | 49436 |
| Product | BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery. |
| Product code | HMX |
| Recalling firm | Becton Dickinson and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2012 |
| FEI number | 1211998 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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