The Stryker LFIT V40 femoral head hip implant devices are being linked to loss of mobility and related serious injuries. These hip implant devices are used in many of Stryker’s modular hip replacement systems and are widely used, worldwide.
Class 2 FDA Hip Implant Recall
The FDA issued a Class 2 Device Recall in 2016 following a high amount of taper lock failure complaints. The recall was terminated in 2017, but complaints continue to surface. A range of serious injuries arose from the Stryker LFIT V40 femoral head hip implants’ taper lock failure. Some of the LFIT V40-related injuries include:
- Pain and inflammation
- Adverse local tissue reaction (ALTRs)
- Joint dislocation, instability, and fractures
- Limb length discrepancy
- Loss of mobility
- And more
If you or a loved one experienced complications after having received Stryker LFIT V40 femoral head hip implants, then please contact our attorneys today for a legal evaluation to determine if you may be eligible to receive financial compensation. There is no obligation or cost for you to receive this evaluation.
Contact us for a Stryker LFIT V40 Settlement Review
At Jason J. Joy & Associates, we provide aggressive legal representation for mass tort medical claims. Our team of attorneys manages Stryker LFIT V40 claims. Contact us today for a complementary and entrusted Stryker LFIT V40 claim review.