ENDOPLUS — Class II medical device recall Z-2265-2013
Terminated recall by Endoplus, Inc., reported 2013-10-02, distributed in FL, TX, VA. Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
| Recall number | Z-2265-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Endoplus, Inc., Mundelein, IL, United States |
| Recall initiated | 2013-07-15 |
| Classified | 2013-09-21 |
| Reported by FDA | 2013-10-02 |
| Terminated | 2016-02-08 |
| Distributed | FL, TX, VA |
| Quantity | 9 units |
| Model numbers | 345VA |
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 for recall
Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2265-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.