Device recall
Z-1212-06: Product is Reprocessed Ethicon Bladeless Trocars. Model: 35NLT, 35NST, 35OL
FDA device recall · Class II · Vanguard Medical Concepts, Inc
Key facts
| Recall number (Z-number) | Z-1212-06 |
|---|---|
| Recall event | 35506 |
| Product | Product is Reprocessed Ethicon Bladeless Trocars. Model: 35NLT, 35NST, 35OL |
| Product code | NLM |
| Recalling firm | Vanguard Medical Concepts, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 31, 2008 |
| 510(k) numbers | K043253 |
| FEI number | 1000132435 |
At a glance
- 1–9 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