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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Product 47 consists of all product under product code: LPH and same usage: Item no: 611004022 MO... | 2 | 03/12/2016 | Zimmer Manufacturing B.V. |
Trilogy® Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated fo... | 2 | 12/24/2014 | Zimmer Manufacturing B.V. |
Bone Screw, self-tapping The Trilogy shells are available in three configurations; uni, multi, and ... | 2 | 12/17/2014 | Zimmer Manufacturing B.V. |
Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW, FULLY THREADED, HEX HEAD 4MM DIAME... | 2 | 07/10/2014 | Zimmer Manufacturing B.V. |
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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