This event is deemed reportable based on the allegations in a lawsuit which, while unsubstantiated, suggest that a reportable event may have occurred during use of atrium medical¿s mesh product.Plaintiff allegedly experienced severe and chronic pain, fistula, infection, sepsis, mesh removal, incontinence, ventral hernia, incisional hernia, inguinal hernia, seroma, adhesions and mental pain and suffering, unincorporated mesh and other complications and injuries.Since this is a legal matter, the case has been turned over to legal counsel and further information obtained through investigation or discovery may fall under the attorney/client and/or work product privilege.However, atrium will supplement this report as appropriate if additional information comes to its attention.
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