DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm, 75mm, 80mm, 85mm, 90mm, 95mm, 105mm); part of the Expert Lateral Femur Nail System and indicated to stabilize Subtrochanteric fractures, Ipsilateral neck/shaft fractures, Femoral shaft fractures, Impending pathologic fractures, and malunions/Non-unions.
FDA Recall Z-1915-2015 · Posted 2015-06-26
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Recalling FirmSynthes, Inc.
Recall StatusTerminated
Product CodeHSB
Date Initiated2015-05-27
Date Terminated2015-12-18
Product Quantity276
Reason for Recall
certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the incorrect insert GP0760-A (Synthes Titanium Buttress Locking Plate System), instead of the correct insert GP0706-E (Synthes Titanium Intramedullary Nails and Components).
Firm Action
DePuy Synthes sent an Urgent Medical Device Safety Notification, dated May 27, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Actions Required:
Please take the following actions:
Review the information listed in this notification.
Forward this notice to anyone in your facility that needs to be informed.
Complete the attached Verification Section (page 3 of this notification). Please include your name, title, address, telephone number and signature in the spaces provided.
Send a copy of the completed Verification Section by:
Fax: (888) 912-2182 or
Scan/email: [email protected]
If the Verification Form is answered on behalf of more than one facility and/or individual, please clearly indicate the name and address of the facility and/or individual in page three (3) of this notification.
Maintain a copy of this notice.
If you have any questions, please call (610)719-5450.
Thank you for your attention to this issue.
Root Cause
Process control
Distribution Pattern
Nationwide Distribution.
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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