Practice

Stryker AccuLIF Recall

Have you had a back surgery with a STRYKER ACCULIF TL or PL cage?

(Stryker AccuLIF TL and PL Cages, or intervertebral body fusion with autograft and/or allogeneic bone graft.)

According to the FDA, Stryker Spine sent an "Urgent Recall Letter and Product Accountability Form" dated July 26, 2016 to all affected customers. For patients who have had an AccuLIF Posterior Lumbar (PL) Expandable Interbody implant, Stryker Spine is recommending routine clinical and radiographic post-operated evaluation. Should the patient report any change in or develop near-onset symptoms, more urgent clinical and radiographic evaluation should be completed.

We are currently investigating legal cases for the recipients of the AccuLIF implants. If you had a surgery that failed as a result of implant collapse, or that will have to be redone because of collapse, then you may be entitled to monetary compensation.

If we take your case, there will be no fee unless we recover for you. Please leave us your name and number, and an attorney will follow up with you shortly.

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La Jolla, California

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La Jolla, California 92037

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