In July 2012, Stryker Orthopaedics issued a voluntary recall of their Rejuvenate and ABG II modular-neck stems. These components are used with many of their hip implant systems in order to create a better fit between the hip implant and the patient’s anatomy. The recall was prompted by numerous reports of safety issues associated with these modular-neck stems. Since January 2012, the FDA has received at least 45 reports of adverse events associated with the Rejuvenate and ABG II modular-neck stems. A spokesperson from Stryker announced that the potential risks associated with these defective medical devices outweigh their benefits, making this recall the best course of action.
Problems Associated with Stryker Modular-Neck Stem Devices
While the Stryker Rejuvenate and ABG II modular-neck stems can be used with either metal or ceramic hip implants, the neck stem components utilize a metal-on-metal design. These components have experienced similar issues that have recently been associated with other metal-on-metal hip implant devices. The friction created when these modular-neck stems move leads to fretting or corrosion, which can release toxic metal debris into the bloodstream. Complications associated with this influx of metal particles in the bloodstream include:- Pain
- Inflammation
- Swelling
- Tissue damage
- Metallosis (metal poisoning)
- Bone loss
- Pseudotumors
- High implant failure rates
Fighting for You
If you have experienced complications or adverse reactions after receiving a hip implant using the Stryker Rejuvenate or ABG II modular-neck stems, you may be entitled to receive compensation for damages such as:- Medical expenses
- Lost income
- Pain and suffering