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U.S. Department of Health and Human Services

Class 2 Device Recall Modular Foot System

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 Class 2 Device Recall Modular Foot Systemsee related information
Date Initiated by FirmMarch 23, 2010
Date PostedJune 10, 2010
Recall Status1 Terminated 3 on September 10, 2012
Recall NumberZ-1784-2010
Recall Event ID 55256
510(K)NumberK073624 
Product Classification Screw, fixation, bone - Product Code HWC
ProductModular Foot System 3.5mm x 22mm Locking Screw M/N: MFT-021-35-22. OrthoHelix Surgical Designs, Inc. Medina, OH 44256. Intended as a guide to normal healing and are not intended to replace normal body structure or bear the weight of the body in the presence of incomplete bone healing.
Code Information Lot Number: 0964081
FEI Number 3000718467
Recalling Firm/
Manufacturer		 Orthohelix Surgical Designs Inc
1065 Medina Rd., Suite 500
Medina OH 44256
For Additional Information Contact
330-869-9582
Manufacturer Reason
for Recall		On 3/9/10 it was discovered that the recalling firm packaged MFT-021-35-24 Screws from lot 0964092 as MFT-021-35-22 lot 0964081.
FDA Determined
Cause 2		Employee error
ActionOrthoHelix Surgical Designs, Inc. issued an "Important Field Correction Notice" dated March 23, 2010 via FedEx overnight. They instructed their customers to inventory their stock for affected product. All affected product will be replaced by the firm. For further information, contact OrthoHelix Surgical Designs, Inc. at 1-330-247-1444.
Quantity in Commerce62 pieces
DistributionNationwide Distribution -- AZ, CA, CO, FL, GA, ID, IL, MD, NC, NJ, NM, NY, OH, OK, PA, SC, TX, UT, VA and WA.
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 = HWC
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