Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K020114 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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3DKnee Baseplates, Size 8, Left, Part # 333-01-108, Lot# A1000003. | 2 | 08/22/2010 | Encore Medical, Lp |
3DKNEE SYSTEM, 3D Knee Tibial Insert-DCM, Sterile, Right, size 4 x 11mm. Encore Medical, LP. Austi... | 2 | 04/26/2010 | Encore Medical, Lp |
3DKNEE Tibial Insert Trial, Size 2, 13mm Right; Part #801-01-640; manufactured by Encore Medical, L.... | 2 | 08/20/2008 | Encore Medical, Lp |
Size 8 right 3DKnee Non-porous Baseplates (Catalog #333-02-108) joint knee replacement. | 2 | 12/29/2005 | Encore Medical, Lp |
3DKnee System, Stemmed Tibia-Nonporous-3D, Size 6, Right, sterile. Manufactured by Encore Orthopead... | 3 | 07/20/2004 | Encore Medical, LP |
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