No conclusions can be made.The patient's attorney alleges adverse patient outcome associated with the hernia mesh used to treat the patient including subsequent surgical intervention and death.No medical records, autopsy report, or death certificate have been provided.No lot number has been provided; therefore, a review of the manufacturing records is not possible.This emdr represents the bard/davol ventralight st mesh (device #2).An additional emdr was submitted to represent the bard/davol mesh - ventralex (device #1).Should additional information be provided, a supplemental emdr will be submitted.
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