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Recall Observatory FDA recall evidence

Device product

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.

Z-0559-2013

November 05, 2012

Class II

Product summary

Firm
Integra LifeSciences Corporation
Event
Event 63776
Status
Terminated
Classification
Class II
Quantity
eight (8) skull clamps were distributed
Official record key
device-enforcement:Z-0559-2013

Official wording

Reason: 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

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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