Attorney alleges that the patient underwent surgery for implant of two unspecified bard/davol 3dmax mesh on (b)(6) 2017 and (b)(6) 2017.As reported, the patient is making a claim for an adverse patient outcome against both devices.Attorney alleges that the patient had subsequent surgical intervention due to the hernia mesh device.It is also alleged that the patient experienced emotional distress, sustained personal injury and the device was defective.
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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 3dmax mesh (device #1).An additional emdr was submitted to represent the bard/davol 3dmax mesh (device #2).Should additional information be provided, a supplemental emdr will be submitted.
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