Class II — Endoplus, Inc.
| Recalling firm | ENDOPLUS |
|---|---|
| Registered facility | ENDOPLUS (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. |
| 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 laparoscopic surgery. |
| Quantity | 81 units |
| Distribution | Distributed in the states of FL, TX, and VA. |
| Initiated | 2013-07-15 |
| Classified | 2013-09-21 |
| Terminated | 2016-02-08 |
| Recall number | Z-2264-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Endoplus, Inc. (Z-2264-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66063/
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