Device recall
Z-3086-2011: Microline Surgical ReNew Laproscopic ControlTip Atraumatic Fenestrated Grasper…
FDA device recall · Class II · Microline Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-3086-2011 |
|---|---|
| Recall event | 59469 |
| Product | Microline Surgical ReNew Laproscopic ControlTip Atraumatic Fenestrated Grasper Forceps Tip Ref: 3642 The ReNew Forceps Laparoscopic Surgical Tips are intended to cut, grasp and dissect various abdominal tissue for use in endoscopic, including laparoscopic surgical procedures where instruments are… |
| Product code | GEI |
| Recalling firm | Microline Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 9, 2011 |
| 510(k) numbers | K981389 |
| FEI number | 1000137656 |
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