| Class 2 Device Recall LCS Complete | |
Date Initiated by Firm | May 26, 2005 |
Date Posted | August 12, 2005 |
Recall Status1 |
Terminated 3 on December 02, 2005 |
Recall Number | Z-1121-05 |
Recall Event ID |
32192 |
PMA Number | P830055S074 |
Product Classification |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing - Product Code NJL
|
Product | Depuy LCS Complete RP insert; polyethylene tibial insert STD, 10 mm; Ref 1294-05-410. |
Code Information |
Lots X1KCA4, X1KCR4, X1TBK4, X3BCL4, X3BCM4, X3KCD4, X3KCL4, X3KCP4, X3KCT4, X66BJ4, X74GH4, X82EL4, Y15A64, Y18BR4, Y18BS4, Y18BT4, Y18CA4, Y18CC4, Y2TDR4, Y3EGD4, Y3EGF4, Y3EGN4, Y41H84, Y41HY4, Y4XC54, Y4XCR4, Y4XDE4, Y4XDF4, Y4XDJ4, Y51F34, Y51F44, Y51F64, Y51F84, Y6DG74, Y6DHD4, Y75KY4, YA8EV4, YA8FF4, YD7C24, YD7C64, YD7CY4, YE7BD4, YE7BH4, YE7BK4 and YJ5B84. |
Recalling Firm/ Manufacturer |
Depuy Orthopaedics, Inc. 700 Orthopaedic Dr Warsaw IN 46582-3994
|
For Additional Information Contact | 800-366-8143 |
Manufacturer Reason for Recall | An incomplete seal on the inner pouch allows exposure to oxygen, which may result in oxidation and would affect long-term performance of the implant. |
FDA Determined Cause 2 | Other |
Quantity in Commerce | 451 |
Distribution | Nationwide, Argentina, Brazil, Canada, Caguas, Colombia, Ireland, Malaysia, Mexico, Panama, Peru, Singapore, South Africa, Sweden, Uruguay and Venezuela. |
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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PMA Database | PMAs with Product Code = NJL
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