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Defective Stryker Replacement Product and Recall

We at the DeVore Acton and Stafford Medical Device Recall Team have been monitoring the Hip Replacement Recalls for product defects.

We have had several of these claims successfully concluded for our clients with them receiving compensation for the medical bill and pain and suffering.

On May 22, 2018, Stryker Orthopedics updated its LFIT V40 Femoral Head Recall to include eight (8) additional catalog numbers.  The original recall occurred in August 2016 and included seven (7) catalog numbers which represented close to 45,000 devices in commerce.

Stryker Orthopedics LFIT V40 Femoral Head Recall

The LFIT V40 is a femoral head that is utilized in hip replacement surgeries. According to the recall, Stryker has received a higher than expected number of femoral head/hip stem dissociations. Severe complications from the LFIT V40 Head include:

The Stryker LFIT V40 is designed to offer a broad range of offsets based on the patients’ needs and can be used interchangeably with Stryker’s entire product line of modular total hip arthroplasty devices. Unfortunately, due to the potential corrosion at the head-neck junction, catastrophic dissociation and metallosis can occur and require emergent revision surgery.

The Unsafe Drug and Medical Device Team at DeVore, Acton & Stafford are investigating the Stryker LFIT CoCr V40 femoral head cases on behalf of patients who were implanted with these devices and have suffered complications. In the event you receive any calls regarding these products, we welcome the opportunity to work with you and your clients.

Call Della Stafford, team leader for DeVore, Acton & Stafford Medical Device Team at 704-275-5616 or email