Endoplus, Inc.: Medical Device Recall in 2013 - (Recall #: Z-2264-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: July 15, 2013

Date Posted: October 2, 2013

Recall Number: Z-2264-2013

Event ID: 66063

Reason for Recall:

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

Status: Terminated

Product Quantity: 81 units

Code Information:

Item: 346VA; Lot Numbers: D3, E3, F3

Distribution Pattern:

Distributed in the states of FL, TX, and VA.

Voluntary or Mandated:

Voluntary: Firm initiated