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U.S. Department of Health and Human Services

Class 2 Device Recall Rod Connector Assembly

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 Class 2 Device Recall Rod Connector Assemblysee related information
Date Initiated by FirmFebruary 01, 2013
Date PostedFebruary 28, 2013
Recall Status1 Terminated 3 on July 01, 2013
Recall NumberZ-0896-2013
Recall Event ID 64265
510(K)NumberK080407 
Product Classification Appliance, fixation, spinal interlaminal - Product Code KWP
ProductFirebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod Connector (52-6700). Product Usage: The connector assemblies allow for rod components to be connected side-to-side, or end-to-end and eliminate the need of rebuilding the entire system with a longer rod in order to include the new vertebral levels.
Code Information Catalog Numbers: 52-6800 & 52-6700; All Lot Numbers
Recalling Firm/
Manufacturer		 Orthofix, Inc
3451 Plano Pkwy
Lewisville TX 75056-9453
For Additional Information ContactDiana Easton
214-937-2509
Manufacturer Reason
for Recall		There is a possibility that the Set Screw (p/n 90-2923) sub-component of the Parallel Rod Connector Assembly (p/n 52-6800) & Axial Rod Connector (p/n 52-6700) may crack during final tightening. Orthofix Inc received six (6) customer complaints related to set screw cracking between November 15, 2010 and December 2012.
FDA Determined
Cause 2		Device Design
ActionOrthofix sent an Urgent Medical Device Recall Notification dated February 1, 2013 to all affected customers. The letter identifed the affected product, problem and actions to be taken. Customers were instructed to identify and remove the affected products from inventory immediately and follow the actions listed in the enclosed Product Return Instructions. For questions or concerns contact Regulatory Affairs at 214-937-2100.
Quantity in Commerce565 total (287 PN 52-6800 and 278 PN 52- 6700)
DistributionWorldwidewide Distribution - USA Nationwide including Puerto Rico and the countries of: Australia, Lebanon, Germany, Spain, Sweden and Israel.
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 = KWP
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