Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2264-2013 — 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

U.S. FDA — Device Enforcement · United States · 2013-07-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2264-2013
Date of alert: 2013-07-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Endoplus, Inc.
Product category: device
Product type: Devices

Reported risk: Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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