Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K934765 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Trilogy F/M Acetabular Shell with Uni-Hole. The Trilogy Acetabular System is indicated for either... | 2 | 02/04/2013 | Zimmer, Inc. |
Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is indicated for either cemen... | 2 | 02/04/2013 | Zimmer, Inc. |
Trilogy Acetabular Shell with Cluster Holes. The Trilogy Acetabular System is indicated for eithe... | 2 | 02/04/2013 | Zimmer, Inc. |
Trilogy Acetabular Shell Spiked. The Trilogy Acetabular System is indicated for either cemented o... | 2 | 02/04/2013 | Zimmer, Inc. |
Zimmer Trilogy Acetabular System Shell with Cluster Holes, Porous, 60mm O.D., Tivanium TI-6AL-4V All... | 2 | 03/19/2008 | Zimmer Inc. |
Zimmer Bone Screw, self tapping, 6.5 mm dia., 20 mm length, tivanium TI-6AL-4V alloy, sterile, Catal... | 2 | 08/03/2006 | Zimmer Inc. |
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