Device recall
Z-2028-2012: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)…
FDA device recall · Class II · Integra Limited
Key facts
| Recall number (Z-number) | Z-2028-2012 |
|---|---|
| Recall event | 62464 |
| Product | Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments are intended for use in laparoscopic gynecological surgery and other operative procedures under endoscopic observations. For use when a rigid endoscopic instrument for grasping, dissecting… |
| Product code | KNF |
| Recalling firm | Integra Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 19, 2013 |
| 510(k) numbers | K103726 |
| FEI number | 3001700044 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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