Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is used for open and closed wedge osteotomies of the medial proximal tibia, lateral proximal tibia, medial and lateral distal femur, treatment of bone and joint deformities, fractures, and malalignment caused by injury or disease such as osteoarthritis.
FDA Recall Z-0473-2014 · Posted 2013-12-10
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Recalling FirmSynthes USA HQ, Inc.
Recall StatusTerminated
Product CodeKTT
Date Initiated2013-10-09
Date Terminated2015-12-18
Product Quantity2912
Reason for Recall
A labeling correction was initiated related to the Surgical Technique Guide J5606-C "TomoFix Osteotomy System" due to the potential for a surgical delay if the surgeon inserts the superior screws at a lesser angle (4 or 6 degrees) and is not aware that those angles are not present.
Firm Action
Synthes sent an Urgent Field Safety Notification/Medical Device Labeling Correction letter dated October 9, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer.
Customers were instructed to exchange the old surgical technique guide version J5606-C with the new version J5606-D provided with this notification.
Review the revised surgical technique guide (Pages 25 & 26).
Forward this Field Safety Notification to anyone in their facility that need to be informed.
If the surgical technique guide has been forwarded to another facility, contact that facility.
Maintain awareness of this notice until all surgical technique guides have been exchanged.
Maintain a copy of this notice.
Customers with questions were instructed to contact their Synthes
Sales Consultant. For questions regarding this recall call 610-719-5000.
Root Cause
Labeling False and Misleading
Distribution Pattern
Worldwide Distribution - USA (nationwide) Canada and Mexico
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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