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U.S. Department of Health and Human Services

Class 2 Device Recall CD Horizon Agile dynamic stabilization device

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 Class 2 Device Recall CD Horizon Agile dynamic stabilization devicesee related information
Date Initiated by FirmNovember 12, 2007
Date PostedSeptember 11, 2008
Recall Status1 Terminated 3 on August 10, 2010
Recall NumberZ-1438-2008
Recall Event ID 46735
510(K)NumberK060615 
Product Classification spinal fixation device - Product Code NQP
ProductMedtronic Sofamor Danek USA, CD Horizon Spinal System Agile Dynamic Stabilization Device, REF 7881570, 15mm, 5.5mm dia x 70mm, size: 15mm x 70mm, not for distribution in the U.S.A. or its territories, for spinal fixation.
Code Information ALL CODES
FEI Number 1000477302
Recalling Firm/
Manufacturer		 Medtronic Sofamor Danek USA Inc
1800 Pyramid Place
Memphis TN 38132-1719
For Additional Information ContactBert Kelly
901-396-1800
Manufacturer Reason
for Recall		Breaks: Shear failure of the cable component of the system.
FDA Determined
Cause 2		Device Design
ActionMedtronic Sofamor Danek initiated its recall on 12/12/2007 by letter to all Risk Managers who received the product at their hospital. Letter were also mailed to surgeons who have implanted the product. Sales Representatives were notified via a conference call and letter to follow-up with thier respective surgeons who have implanted the product to verify that their surgeon received the communication of the recall and that they are aware that patient monitoring is recommended.
Quantity in Commerce136 units
DistributionWorldwide Distribution: USA, Canada, India, Venezuela, Netherlands, Chile, Brazil, and Australia.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = NQP
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