Date of event is estimated.Date of explant is estimated.During processing of this complaint, attempts were made to obtain patient¿s weight.Further information was requested but not received.Based on the information provided a device problem was not identified, as a result a conclusive cause for the reported patient effect, and the relationship to the product, if any, cannot be determined.
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Related manufacturer reference number 1627487-2020-33252.It was reported that patient was paralyzed post explant.Reportedly, patient was explanted due to infection at the lead and ipg site (related manufacturer reference numbers 1627487-2020-33247, 1627487-2020-33248, 1627487-2020-33250).
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