Device recall
Z-0051-2014: Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog…
FDA device recall · Class II · Synergetics Inc
Key facts
| Recall number (Z-number) | Z-0051-2014 |
|---|---|
| Recall event | 65969 |
| Product | Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge cannula used in vitreoretinal surgery. |
| Product code | HMX |
| Recalling firm | Synergetics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 7, 2014 |
| FEI number | 1000119053 |
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