Device recall
Z-2690-2011: LiNA Loop Endoscopic Monopolar Loop for LSH (Laparoscopic Supracervical…
FDA device recall · Class II · LINA Medical ApS
Key facts
| Recall number (Z-number) | Z-2690-2011 |
|---|---|
| Recall event | 58444 |
| Product | LiNA Loop Endoscopic Monopolar Loop for LSH (Laparoscopic Supracervical Hysterectomy). Large loop, 8mm connector, 1 X REF: EL-200-8 and 10 X REF: EL-200-8, Manufactured by LiNA Medical ApS, Surgery Division. |
| Product code | KNF |
| Recalling firm | LINA Medical ApS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 23, 2012 |
| 510(k) numbers | K070315 |
| FEI number | 3002626775 |
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