Microline Surgical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1986-2014)

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 Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221

Product Classification:

Class II

Date Initiated: May 12, 2014

Date Posted: July 9, 2014

Recall Number: Z-1986-2014

Event ID: 68495

Reason for Recall:

Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw

Status: Terminated

Product Quantity: 150 units

Code Information:

Lot Numbers: 00115342

Distribution Pattern:

Worldwide Distribution-USA including the states of CA, HI, ID, MA, MI, MS, PA, TN, UT, and TX. and the countries of Belgium, France, Ireland, Germany, Indonesia, Korea, Norway, Saudi Arabia, Switzerland, Turkey, and UK.

Voluntary or Mandated:

Voluntary: Firm initiated