Integra LifeSciences Corporation: Medical Device Recall in 2012 - (Recall #: Z-0559-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

MAYFIELD Composite Series Skull Clamps, Model A3059, 510(k) #K120633. The MAYFIELD Skull Clamps (A3059) are indicated for use in open and percutaneous craniotomies, as well as spinal surgery when rigid skeletal fixation is necessary.

Product Classification:

Class II

Date Initiated: November 5, 2012

Date Posted: December 26, 2012

Recall Number: Z-0559-2013

Event ID: 63776

Reason for Recall:

An investigation of an adverse trend of complaints conducted by Integra LifeSciences identified various product performance issues which could impact the functionality of the firm's Mayfield Composite Series Base Units and Mayfield Skull Clamps. In order to prevent additional complaint reports, the firm decided to recall and replace certain lot codes of the Base Units and Skull Clamps that were d

Status: Terminated

Product Quantity: eight (8) skull clamps were distributed

Code Information:

The recalled product is identified with the Lot Numbers: 096455 and 097546.

Distribution Pattern:

Nationwide Distribution including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, IN, KY, MA, MD, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA TN, TX, UT, VA, WA and WI.

Voluntary or Mandated:

Voluntary: Firm initiated