Synthes Application Instrument Sternal Zip Flex System intended for use in primary or secondary closure/repair of the sternum following sternotomy or fracture of the sternum to stabilize the sternum and promote fusion
FDA Recall Z-0114-2014 · Posted 2013-10-30
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Recalling FirmSynthes USA HQ, Inc.
Recall StatusTerminated
Product CodeJDQ
Date Initiated2013-08-13
Date Terminated2016-08-18
Product Quantity319
Reason for Recall
When using the 1st generation Zip Fix Application Instrument it is possible to cut the implant while the tensioning trigger is being squeezed which could lead to loosening of the implant.
Firm Action
Synthes sent a Urgent Medical Device Notification dated August 13, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Action to be taken: This notification is to make you aware of the issue and the importance of completely releasing the tensioning trigger before cutting the implant. Please take the following action:
"To ensure your receipt and understanding of this information, Please complete the verification section of this letter and return to Synthes by either of the following methods:
" Fax: 1-888-352-9616 or
" Scan/email: [email protected]
If you have any questions, please call 610-719-5450 or contact your Synthes Sales Consultant.
Root Cause
Labeling False and Misleading
Distribution Pattern
Worldwide Distribution - US (nationwide) and country of 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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