Zimmer Manufacturing B.V. - NexGen Complete Knee Solution MIS Total Knee Procedure Stemmed Tibial Component, Precoat - Class 2 Recall
***LOT***NexGen¿ Complete Knee Solution***MIS Total Knee Procedure***Stemmed***Tibial Component***Precoat***Fixed Bearing***Size*** NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis. The device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis; Collagen disorders, and/or avascular necrosis of the femoral condyle; Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy; Moderate valgus, va...
Source: Medical Device Recalls - June 28, 2014 Category: Medical Equipment Source Type: alerts
RHEUMATOID ARTHRITIS NOSODE (Atp (Adenosine Triphosphate Disodium), Malic Acid, Natrum Oxalaceticum, Oroticum Acidum, Riboflavinum, Apiolum, Cinnamic Acid, Dhea (Dehydroepiandrosterone),) Liquid [Deseret Biologicals, Inc.]
Updated Date: Jun 23, 2014 EST (Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST))
Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST) - June 23, 2014 Category: Drugs & Pharmacology Source Type: alerts
Ortho Development Corporation - PSC Femoral Nonporous Rt Sz 6 - Class 2 Recall
PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Product Usage: 1. Loss of joint configuration and joint function. 2. Osteoarthritis of the knee joint. 3. Rheumatoid arthritis of the knee joint. 4. Post-traumatic arthritis of the knee joint. 5. Valgus, varus, or flexion deformities. 6. Revision procedures where other treatments or devices have failed. The Balanced Knee¿ System and Balanced Knee¿ Revision System are intended for total knee arthroplasty procedures. The Balanced Knee¿ System is indicated in the salvage of previously failed surgical attempts where femoral bone loss does not require the ...
Source: Medical Device Recalls - May 14, 2014 Category: Medical Equipment Source Type: alerts
Stryker Howmedica Osteonics Corp. - Class 2 Recall
Stryker Orthopaedics Product Usage: The citation TMZF HA stem is indicated for cementless primary hip surgery in cases of non-inflammatory degenerative joint disease including osteoarthritis, avascular necrosis, rheumatoid arthritis, and correction of functional deformity. Additionally it can be used in treatment of nonunion, and femoral neck and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques. It is also indicated for use in revision procedures where other treatments or devices have failed. 1) Citation TMZF HA 132 degrees Neck Angle V40 Hip Stem - ...
Source: Medical Device Recalls - April 3, 2014 Category: Medical Equipment Source Type: alerts
Smith & Nephew Inc - Reflection(R) Interfit(TM) Shell, 52 MM OD, 3 HOLE - Class 2 Recall
Reflection(R) Interfit(TM) Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2014 Category: Medical Equipment Source Type: alerts
