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Zimmer, Inc. - Zimmer Trabecular Metal Total Ankle Tibial Base and Talar Components - Class 2 Recall
Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular Metal Total Ankle is indicated as a total ankle replacement in primary or revision surgery for patients with: " Rheumatoid arthritis. " Post-traumatic arthritis. " Degenerative arthritis. This device is intended for cemented use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 11, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - Zimmer Trabecular Metal Total Ankle Tibial Base and Talar Components - Class 2 Recall
Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular Metal Total Ankle is indicated as a total ankle replacement in primary or revision surgery for patients with: " Rheumatoid arthritis. " Post-traumatic arthritis. " Degenerative arthritis. This device is intended for cemented use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 11, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - Zimmer Trabecular Metal Total Ankle Tibial Base and Talar Components - Class 2 Recall
Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular Metal Total Ankle is indicated as a total ankle replacement in primary or revision surgery for patients with: " Rheumatoid arthritis. " Post-traumatic arthritis. " Degenerative arthritis. This device is intended for cemented use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 11, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - NexGen Complete Knee Solution - Class 2 Recall
NexGen¿ Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - NexGen Complete Knee Solution - Class 2 Recall
NexGen¿ Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - NexGen Complete Knee Solution - Class 2 Recall
NexGen¿ Complete Knee Solution CR Articular Surface Provisional-Yellow 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - NexGen Complete Knee Solution - Class 2 Recall
NexGen¿ Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Zimmer, Inc. - NexGen Complete Knee Solution - Class 2 Recall
NexGen¿ Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Stelkast Co - SC2316, Distal Femoral Augment with Screw - Class 2 Recall
SC2316, Distal Femoral Augment with Screw Total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis and/or post-traumatic degenerative problems and revision of failed previous reconstructions. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 4, 2013 Category: Medical Equipment Source Type: alerts

Synthes USA HQ, Inc. - Class 2 Recall
Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the Multi Vector Distractor which cis used for mandibular bone lengthening, including conditions such as congenital mandibular deficiencies or post-traumatic defects. The Multi Vector Distractor can be utilized to perform bone transport procedures as an alternative to bone grafts and free flaps. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 18, 2013 Category: Medical Equipment Source Type: alerts

Synthes USA HQ, Inc. - Synthes Craniomaxillofacial (CMF) Distraction System - Class 2 Recall
Synthes CMF Distraction System The product is intended for use as a bone stabilizer and lengthening (and/or transport) device for correction of congenital deficiencies or post-traumatic defects of the mandibular body and ramus, where gradual bone distraction is required. It is intended for single use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 13, 2013 Category: Medical Equipment Source Type: alerts