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 not reported) dose, frequency and therapy dates not reported, additional dosage information included: Dose series: 1, for covid-19 prophylaxis. The batch number was not reported. The company is unable to perform follow up to request batch or 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 a product quality complaint: Product Complaint 90000347802. 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. This report was non-serious.