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Stryker Howmedica Osteonics Corp. recalls Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer
Recalled September 21, 2016 · FDA recall Z-2792-2016 · Stryker Howmedica Osteonics
Hazard
Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field. · FDA Class II
Units
1 unit in total
Sold at
US distribution to state of: CA.
Description
Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.
Product
Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either an antegrade or a retrograde approach to repair fractures of the femur. (1) Open and closed femoral fractures, (2) Pseudoarthrosis and correction, (3) osteotomy, (4) Pathologic fractures, impending pathologic fractures, and tumor resections, (5) Supracondylar fractures, including those with intra-articular extension, (6) Ipsilateral femur fractures, (7) Fractures proximal to a total knee arthroplasty, (8) Fractures distal to a hip joint and (9) Non-unions and malunions
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →