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Catalog Number UNKAA077 |
Device Problems
Defective Device (2588); Insufficient Information (3190)
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Patient Problems
Death (1802); Injury (2348); Disability (2371)
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Event Date 06/20/2019 |
Event Type
Death
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Manufacturer Narrative
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At this time no conclusions can be made.The patient's attorney alleges wrongful death of the patient and general allegations for past, present, and future damages, including but not limited to, mental and physical pain and suffering for severe and permanent personal injuries sustained by the patient, however, no details have been provided.No lot number has been provided; therefore, a review of the manufacturing records is not possible.Should additional information be provided a supplemental emdr will be submitted.Not returned.
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Event Description
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Attorney alleges that the patient underwent surgery for implant of an unspecified bard/davol ventralex on (b)(6) 2018.As reported, the patient is making a claim for an adverse patient outcome against the ventralex.It is alleged that the patient sustained unspecified injuries on (b)(6) 2019.Attorney alleges that ¿on (b)(6) 2019, the patient passed away due to defendants' negligence, defective product, defective design, failure to warn, and/or other wrongful acts.¿ attorney also alleges general allegations for "past, present, and future damages, including but not limited to, mental and physical pain and suffering for severe and permanent personal injuries sustained by the patient.¿ it is also alleged that the patient experienced emotional distress and the device was defective.
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Search Alerts/Recalls
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