Endoplus, Inc. recalls ENDOPLUS; Precision Laparoscopic Instruments; REF 345VA; Description 5 mm Traumatic Grasper S/A, Standard; Non-sterile

Recalled October 2, 2013 · FDA recall Z-2265-2013 · Endoplus

Hazard

Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. · FDA Class II

Units

9 units

Sold at

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

Description

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

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.

Manufacturer(s)

Endoplus, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →