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Endoplus, Inc. recalls ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm Atraumatic Grasper S/A, Standard; Non-sterile
Recalled October 2, 2013 · FDA recall Z-2264-2013 · Endoplus
Hazard
Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. · FDA Class II
Units
81 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 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.
Manufacturer(s)
Endoplus, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →