Attorney alleges that the patient underwent surgery for implant of unspecified bard/davol kugel hernia patch, bard/davol marlex (bard flat mesh) and bard/davol ventralight st on (b)(6) 2013.As reported, the patient is making a claim for an adverse patient outcome against all the 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 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 ventralight st mesh (device #3).An additional emdr was submitted to represent the bard/davol kugel patch (device #1) and bard/davol marlex (bard flat mesh) (device #2).Should additional information be provided, a supplemental emdr will be submitted.The information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.Not returned.
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