No conclusions can be made.The patient's attorney alleges adverse patient outcome associated with the hernia mesh used to treat the patient.The patient's attorney alleges that the patient had subsequent surgical intervention; however, no details 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).Additional emdrs were submitted to represent the two bard/davol ventralight st meshes (device #1, device #3).Should additional information be provided, a supplemental emdr will be submitted.Not returned.
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