Device recall
Z-1986-2014: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
FDA device recall · Class II · Microline Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1986-2014 |
|---|---|
| Recall event | 68495 |
| Product | Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221 |
| Product code | GEI |
| Recalling firm | Microline Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 13, 2015 |
| 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