Device recall
Z-2161-2011: BD Visitec High Viscosity Injector 4mm [Hammer].90 (20G) Catalog Number: 585208…
FDA device recall · Class II · Becton Dickinson and Company
Key facts
| Recall number (Z-number) | Z-2161-2011 |
|---|---|
| Recall event | 57472 |
| Product | BD Visitec High Viscosity Injector 4mm [Hammer] .90 (20G) Catalog Number: 585208 High Viscosity Injectors are used during retinal surgery for fluid infusion. A High Viscosity Injector is placed into the sclera and temporarily sutured into place. |
| Product code | HMX |
| Recalling firm | Becton Dickinson and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 3, 2013 |
| 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