Background and Objectives: Convalescent COVID-19 plasma (CCP) was developed and used worldwide as a treatment option by supplying passive immunity. Adult studies suggest administering high-titer CCP early in the disease course of patients who are expected to be antibody-negative; however, pediatric experience is limited. We created a multi-institutional registry to characterize pediatric patients (<18 years) who received CCP and to assess the safety of this intervention.Methods: A REDCap survey was distributed. The registry collected deidentified data including demographic information (age, gender, and underlying conditions), COVID-19 disease features and concurrent treatments, CCP transfusion and safety events, and therapy response.Abbreviations: CCP, COVID-19 convalescent plasma; CTCAE, common terminology criteria for adverse events; EBV, estimated blood volume; FDA, United States Food and Drug Administration; MIS-C, multisystem inflammatory syndrome in children; REDCap, research electronic data capture.