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U.S. Department of Health and Human Services

Class 2 Device Recall Conformis

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  Class 2 Device Recall Conformis see related information
Date Initiated by Firm July 17, 2012
Date Posting Updated August 17, 2012
Recall Status1 Terminated 3 on February 27, 2013
Recall Number Z-2222-2012
Recall Event ID 62576
510(K)Number K103117  
Product Classification Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
Product Conformis iTotal CR-Cruciate Retaining Knee Replacement System
Model Numbers:
M57250600010 iTotal CR, Left Knee
M57250600020 iTotal CR, Right Knee

Product Usage : Usage:
The iTotal CR Knee Replacement System (KRS) is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a prosthetic device that treats only one or two of the three knee compartments, such as a unicondylar, patello-femoral or bi-compartmental prosthesis.



Code Information All serial numbers
Recalling Firm/
Manufacturer
Conformis Inc
1 North Ave
Suite B
Burlington MA 01803-3305
Manufacturer Reason
for Recall
Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of Total CR Poly Insertion Technique
FDA Determined
Cause 2
Device Design
Action ConforMIS sent an Urgent Field Safety Notice letter dated July 5, 2012 to all affected customers. The letter identified the affected product, problem and actions to be taken. An Addendum is included that provided updates to the Surgical Technique Guide. The updated technique guide will be delivered to all iTotal surgeons along with an on-site vist from ConforMIS sales representative. Customers were instructed to place the Surgical Technique Guide Addendum alongside the surgical plan, it puts the information in a highly visible location for the surgeon to review prior to the surgical procedure. Customers were asked to sign the communication verification form attached. For any questions regarding this notice, please contact your local ConforMIS representative or MDSS GmbH, Tel.: +49-511-62628630, info@mdss.com.
Quantity in Commerce 1427 units
Distribution Worldwide Distribution - US Nationwide and the country of Germany
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.
510(K) Database 510(K)s with Product Code = JWH and Original Applicant = CONFORMIS, INC.
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