Device recall
Z-2137-2012: SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER Surgical…
FDA device recall · Class II · Transenterix, Inc
Key facts
| Recall number (Z-number) | Z-2137-2012 |
|---|---|
| Recall event | 62583 |
| Product | SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER Surgical Instruments are intended for use in minimally invasive surgical procedures for grasping, mobilizing, dissecting, retracting, cutting, cauterizing, ligating, suction/irrigation and other manipulation of tissues and vessels during a… |
| Product code | GCJ |
| Recalling firm | Transenterix, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 27, 2013 |
| 510(k) numbers | K091697 |
| FEI number | 3007593944 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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