Device recall
Z-0884-2014: 23ga Endo Illuminator (Eckardt Trocar Compatible), Synergetics, inc., length 8.0…
FDA device recall · Class II · Synergetics Inc
Key facts
| Recall number (Z-number) | Z-0884-2014 |
|---|---|
| Recall event | 67147 |
| Product | 23ga Endo Illuminator (Eckardt Trocar Compatible), Synergetics, inc., length 8.0 ft, sterile / EO, 56.02.23P Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO. |
| Product code | HQB |
| Recalling firm | Synergetics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 25, 2015 |
| FEI number | 1000119053 |
At a glance
- None Linked 510(k)s
- 10–99 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