A non-stryker user surgeon reached out from a teaching facility asking if a femoral head component that he revised over a year ago was a part of lfit v40 recall from dates 2011-2016.After looking up the product number and lot code with the sales manager through our resources, the item in question was determined to not be a part of the recall.He reported trunnion wear and adverse tissue reactions.Informed that he revised the femoral and acetabular components to another companies implants and disposed of the implants removed.
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