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U.S. Department of Health and Human Services

Class 2 Device Recall Preservation

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 Class 2 Device Recall Preservationsee related information
Date Initiated by FirmMay 26, 2005
Date PostedAugust 12, 2005
Recall Status1 Terminated 3 on December 02, 2005
Recall NumberZ-1149-05
Recall Event ID 32192
510(K)NumberK010810 
Product Classification Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing - Product Code NJL
ProductDepuy Preservation Uni Knee All Poly Tibial; polyethylene tibial insert LM/RL, Sz 3, 7.0 mm; Ref 1498-12-306.
Code Information Lots X91B34, Y54EF4, Y54EG4, Y5EFM4, Y5EFP4, Y5GEJ4, Y68K14, Y68K74, Y68K84 and Y68KX4.
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 Commerce117
DistributionNationwide, Argentina, Brazil, Canada, Caguas, Colombia, Ireland, Malaysia, Mexico, Panama, Peru, Singapore, South Africa, Sweden, Uruguay and Venezuela.
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 = NJL
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