Microline Surgical recalls Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasp

Recalled May 28, 2014 · FDA recall Z-1635-2014 · Microline Surgical

Hazard

Grasper jaw may break when force is applied to the jaw · FDA Class II

Units

540 units

Sold at

Worldwide Distribution - US including the states of TX, IL, TN and NY, and the country of Chile.

Description

Grasper jaw may break when force is applied to the jaw

Product

Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper Forceps Tips are intended to cut, grasp, and dissect various abdominal tissue for use in endoscopic, including laproscopic surgical procedures where instruments are introduced onto the body through a cannula.

Manufacturer(s)

Microline Surgical

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