| Class 2 Device Recall UKNEE Patella | |
Date Initiated by Firm | February 20, 2013 |
Date Posted | May 24, 2013 |
Recall Status1 |
Terminated 3 on March 26, 2014 |
Recall Number | Z-1380-2013 |
Recall Event ID |
64588 |
510(K)Number | K103733 |
Product Classification |
Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
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Product | UKNEE Patella,small 2401-1010
UKNEE Patella,medium 2401-1020
UKNEE Patella,large 2401-1030
UKNEE Patella,X-large 2401-1040
UKNEE Onset Patella, 3 pegs, x-small 2403-1010
UKNEE Onset Patella, 3 pegs, small 2403-1020
UKNEE Onset Patella, 3 pegs, medium 2403-1030
UKNEE Onset Patella, 3 pegs, large 2403-1040
UKNEE Onset Patella, 3 pegs,X-large 2403-1050
Variety of hip and knee implants and instruments, multiple uses. |
Code Information |
Catalog No. 2401-1010 2401-1020 2401-1030 2401-1040 2403-1010 2403-1020 2403-1030 2403-1040 2403-1050 |
Recalling Firm/ Manufacturer |
Orthopedic Alliance LLC 26157 Jefferson Ave Murrieta CA 92562-9561
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For Additional Information Contact | 909-304-9001 |
Manufacturer Reason for Recall | The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Orthopedic Alliance because the directions for use and surgical techniques were not being provided to every physician
and for every surgery. |
FDA Determined Cause 2 | Labeling design |
Action | A recall letter dated 3/8/13 was sent to all customers who purchased loaner bins and sterilization trays for implants and instruments from Orthopedic Alliance. The letter informed the customers of the problem identified
and the actions to be taken. Customers are instructed to call the office at the number (951) 304-9001 if they are requesting paper copies of any of the literature. |
Quantity in Commerce | 57 units |
Distribution | Nationwide Distribution including the states of CA, MD, TX, NV, and WI. |
Total Product Life Cycle | TPLC Device Report |
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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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510(K) Database | 510(K)s with Product Code = JWH
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