deadly vaccine; This spontaneous report received from a consumer by a company representative concerned a patient of unspecified age and sex. Additional reporter noted as Lawyer. Document was received in the form Legal Summons and Complaint and EZ report. The patient’s height and weight were not reported. Age at time of vaccination was unknown. No past medical history, concurrent conditions or pre-existing medical conditions were reported. The patient received janssen covid-19 vaccine (suspension for injection, intramuscular, batch number: Unknown) dose, frequency and therapy dates not reported, additional dosage information included: Dose series: 1, for covid-19 prophylaxis. The batch number was not reported. Company was unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the patient experienced deadly vaccine. After taking COVID-19 shot. (dose series is 1) The action taken with janssen covid-19 vaccine was not applicable. The outcome of deadly vaccine was not reported. This report was associated with product quality complaints: Product Complaint 90000347962; 90000347798. Investigation Results: Undetermined. Product identification information and/or physical evidence, including field sample or photograph to conduct a root cause investigation was not available at the time of this assessment. Root cause and disposition determinations were assessed based on available information. Although a definitive root cause could not be determined for this case, this complaint record will be included in the periodic product quality complaint trending. Verified signals are assessed as per TV-WI-14276. No further action is required at this time. This report was non-serious.