FDA Device recall Z-2265-2013
ENDOPLUS
- FDA Device
- Class II
- terminated
- Published 2013-10-02
On 2013-10-02 the FDA classified a Class II recall of ENDOPLUS by Endoplus, citing multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2265-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-15 |
| Published | 2013-10-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Endoplus |
| Distribution | FL, TX, VA |
Product
ENDOPLUS; Precision Laparoscopic Instruments; REF 345VA; Description 5 mm Traumatic 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 laparoscopic surgery.
Reason
Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
Identifiers
| code_info | Item: 345VA; Lot Number: F3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2265-2013%22
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