Recall Z-0498-2010

Alphatec Spine, Inc. · initiated January 28, 2009

Terminated

Product

ILLICO Posterior Thoracolumbar Access Retractor, Part Number: 73520 The ILLICO Posterior Thoracolumbar Access Retractor is an instrument that is intended for use in a minimally invasive approach for surgical procedures. The retractor allows retraction of tissue through combination of articulating blades. Device will serve to provide access for surgeons to surgical site.

Codes / lots: Lot number: 5271901

Reason for recall

The recall was initiated after Alphatec Spine received a complaint on the ILLICO Posterior Thoracolumbar access retractor. It was reported that one of the retractor arms in the retractor broke during surgery.

FDA-determined cause: Device Design

Action taken

On January 28, 2009 Alphatec Spine contacted their domestic consignees via telephone and the international consignee was contacted via telephone and electronic mail. Alphatec Spine's telephone call consisted of informing the consignees of the product affected, the problem, what actions needed to be taken and what action Alphatec Spine would take to arrange for pick-up of the affected products.

Details

Recall number
Z-0498-2010
Initiated
January 28, 2009
Posted by FDA
December 11, 2009
Terminated
December 22, 2009
Product code
GAD – Retractor
Quantity
14
Distribution
AZ, CA, OR, TX, and Tokyo, Japan.
Recalling firm
Alphatec Spine, Inc., Carlsbad, CA

Official FDA recall record