Microline Surgical: Medical Device Recall in 2014 - (Recall #: Z-1635-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: April 14, 2014

Date Posted: May 28, 2014

Recall Number: Z-1635-2014

Event ID: 68012

Reason for Recall:

Grasper jaw may break when force is applied to the jaw

Status: Terminated

Product Quantity: 540 units

Code Information:

Lot Numbers: 00116169 and 00115866

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated