Exactech
exactech
Exactech® has recalled 147,000+ defective joint replacement products (Hip, Knee, Ankle). The FDA has classified this as a Class II recall, meaning that exposure to the product may cause temporary or medically reversible health consequences. An issue with the products' packaging may cause oxidation and cause the replacement to wear out faster than expected. Over time, this can severely degrade the mechanical properties of the polyethylene inserts. This plastic component acts as cartilage, or a cushion, between the metal components of the new knee joint. Ultimately, these recalled products can lead to costly revision surgery and further injuries. If you or a loved one have an Exactech ankle, hip, or knee implant contact us immediately for a free consultation.
recalled products
The massive recall includes certain Optetrak®, Optetrak Logic®, Truliant®, and Vantage® products made by Exactech.
Common symptoms of a loose ankle, knee, or hip replacement can be so painful to manage that corrective revision surgery is required to repair or replace the defective insert. See if your implant is listed below.
- Optetrak All-polyethylene CR Tibial Components
- Optetrak All-polyethylene PS Tibial Components
- Optetrak CR Tibial Inserts
- Optetrak CR Slope Tibial Inserts
- Optetrak PS Tibial Inserts
- Optetrak HI-FLEX PS Tibial Inserts
- Optetrak Logic CR Tibial Inserts
- Optetrak Logic CR Slope Tibial Inserts
- Optetrak Logic CRC Tibial Inserts
- Optetrak Logic PS Tibial Inserts
- Optetrak Logic PSC Tibial Inserts
- Optetrak Logic CC Tibial Inserts
- Truliant CR Tibial Inserts
- Truliant CR Slope Tibial Inserts
- Truliant CRC Tibial Inserts
- Truliant PS Tibial Inserts
- Truliant PSC Tibial Inserts
- SystemOne (Q-Series)
- Vantage Fixed-Bearing Liner Component
common symptoms
- Bone Loss or Osteolysis
- Grinding
- Implant Loosening
- Inability to Bear Weight
- Joint Instability
- Limited Mobility
- Pain
- Swelling
- Stiffness
- Tissue Damage