Device recall
Z-2264-2013: ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm…
FDA device recall · Class II · Endoplus, Inc.
Key facts
| Recall number (Z-number) | Z-2264-2013 |
|---|---|
| Recall event | 66063 |
| Product | ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm Atraumatic Grasper S/A, Standard; Non-sterile; Manufactured by Endoplus; 750 Tower Rd., Suite A, Mundelein, IL 60060 USA. Intended for grasping, dissecting, retraction, clamping in conjunction with the laparoscopic during… |
| Product code | GCJ |
| Recalling firm | Endoplus, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2016 |
| 510(k) numbers | K925079 |
| FEI number | 3000719482 |
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