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U.S. Department of Health and Human Services

Class 2 Device Recall Synthes Recon Locking Aiming Arm for Lateral Entry Femoral NailsEX and the Thumb Screw for the Aim

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  Class 2 Device Recall Synthes Recon Locking Aiming Arm for Lateral Entry Femoral NailsEX and the Thumb Screw for the Aim see related information
Date Initiated by Firm February 17, 2015
Date Posted March 16, 2015
Recall Status1 Terminated 3 on August 26, 2016
Recall Number Z-1281-2015
Recall Event ID 70455
Product Classification Guide, surgical, instrument - Product Code FZX
Product Thumb Screw for the Synthes Recon Locking Aiming Arm for Lateral Entry Femoral Nails-EX (part number 03.010.048) and the Thumb Screw for the Aiming Arm for Titanium Cannulated Tibial Nails-EX (part number 03.010.052).


The Recon Locking Aiming Arm for Lateral Entry Femoral Recon Nails- EX is used when locking the Femoral Nail-EX. The Aiming Arm for Titanium (TI) Cannulated Tibial Nails-EX is used when locking the Tibial Nail-EX.
Code Information Part numbers:03.010.048 and 03.010.052 with  Lot Numbers:  4874015 4874021 4927262 4954481 4963192 4874016 4874022 4944750 4957586 4963193 4784017 4899564 4944751 4957587 4972003 4874018 4899565 4954478 4957588 4972004 4874019 4927260 4954479 4957589  4874020 4927261 4954480 4963190  4922533 4922975 4981158  4922970 4923015 4981159  4922971 4977241 4981160  4922972 4977242 4981162  4922973 4981156 5035905  4922974 4981157 5035906  
Recalling Firm/
Manufacturer		 Synthes, Inc.
1302 Wrights Ln E
West Chester PA 19380-3417
For Additional Information Contact Customer Support
610-719-5000
Manufacturer Reason
for Recall		 For certain lots, the incorrect raw material of annealed 17-4PH Stainless Steel was used instead of the correct material of heat-treated 304 Stainless Steel. This may lead to stress-corrosion cracking, which can lead to surgical delay or unintended debris entering the surgical site.
FDA Determined
Cause 2		 Process control
Action An Urgent Notice: Medical Device Recall, dated February 17, 2015, was sent to all direct consignees and sales consultants instructing them to take the following actions: Take note of the quantity of affected parts in your possession, and then follow ONE of the options for replacement of the affected product: Option 1: Call DePuy Synthes Repair Department at 1-800-288-6698 to schedule a repair for the affected products. Complete the Verification Section following the instructions provided and send a copy of the completed Verification Section to DePuy Synthes by: Fax: 866-723-2823 or Scan/e-mail: Synthes6734@stericycle.com Option 2: Call DePuy Synthes Repair Department at 1-800-288-6698 to order repair part. The replacement part will be sent directly to your facility. Questions should be directed to 610-719-5450 or a local DePuy Synthes sales consultant.
Quantity in Commerce 183
Distribution Nationwide Distribution
Total Product Life Cycle TPLC 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.
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