FDA Recall Terminated

Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar pedical screw system designed to provide flexibility biomechanical performance and a solution to complex posterior pathological challenges.

Recall: Z-0384-2014 · Initiated July 31, 2013

Recall

Recall Number
Z-0384-2014
Event Number
66415
Firm
Synthes USA HQ, Inc.
FEI Number
3005180112
Product Code
LXH
Status
Terminated
Root Cause
Labeling design
Initiated
July 31, 2013
Posted
November 22, 2013
Terminated
August 31, 2015
Address
1302 Wrights Ln E, West Chester, PA, 19380-3417

Description

Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar pedical screw system designed to provide flexibility biomechanical performance and a solution to complex posterior pathological challenges.

Reason

Synthes became aware that during a procedure using the Matrix Threaded Persuader, the Reduction Insert malfunctioned causing pieces to break off. Once there is a breakage to the Reduction Insert it will not allow the instrument to function as required.

Action

The firm, Synthes, sent an "URGENT NOTICE: MEDICAL DEVICE RECALL" letter dated July 31, 2013 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to review your inventory and immediately remove the affected lots from stock; If you do have the affected devices, contact Synthes at 1-800-479-6329 to obtain the RA# and return the product to with completed form to Credit/Returns, Synthes, 1101 Synthes Avenue, Monument, CO 80132; complete and sign the Return Receipt Requested form via fax at 1-888-731-7955 or email to: [email protected], even if you do not have the affected product. If you have questions, please call 610-719-5450.

Distribution

Worldwide distribution: US (nationwide) and countries of Canada and Switzerland.

Quantity

634