¿date of event¿ is estimated.During processing of this complaint, attempt was made to obtain complete event information and patient weight.The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Related manufacturer reference numbers: 1627487-2020-04943, 1627487-2020-04944.It was reported that patient experienced heating at ipg site and shocking.As a result, the surgical intervention occurred during which the system was explanted.The date of explant is unknown.
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