RecallDepth

Solanas Posterior Stabilization System Part Number: 63920. Solanas Posterior Stabilization System facilitates the surgical correction of spinal deformities by providing temporary internal fixation and stabilization during bone graft healing and/or fusion mass development. The Solanas Posterior Stabilization System is a spinal fixation system intended to improve stability of the cervical and thoracolumbar area of the spine (C1-T3).

This recall has been terminated (originally issued January 31, 2012).

Company
Alphatec Spine, Inc.
Recall Initiated
November 1, 2010
Posted
January 31, 2012
Terminated
January 31, 2012
Recall Number
Z-0932-2012
Quantity
27 units
Firm Location
Carlsbad, CA
Official Source
View on FDA website ↗

Reason for Recall

These lots were not manufactured correctly in that the instrument does not have the durability required to repeatedly perform over its full service life and, therefore, may experience breakage in the tips.

Distribution

Nationwide Distribution-including the states of CA, CT, FL, GA, NC, NE, NJ, TX, and UT.

Lot / Code Info

Lot Numbers: 608227B, 609867B, 609870B, 609882B, 609897B, 609971B

Root Cause

Device Design

Action Taken

Alphatec Spine contacted all affected customers via telephone. The communication included discussion of the product, problem, and actions to be taken by the customers. Customers were instructed to remove the affected product from inventory and to return the product to the firm. Arrangements were made for replacement product to be sent to the customers. Contact the firm at 1-800-922-1356 for questions regarding this recall.

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