The modern era of blood transfusions was ushered in by the discovery of human red cell groups by Shattock (1) in 1900 and Landsteiner (2) in 1901. Grouping was later systematized by Jansky (3) and Moss (4). In the course of a few years the paraffined tube method of KimptonBrown (5), the multiple syringe technic of Lindeman (6) and the 4-way stopcock apparatus of Unger (7) came into general use in hospitals for direct transfusions. All of these methods required speed in transferring blood from donor to recipient because of the dangers of clotting.Agote (8) and Lewisohn (9) introduced sodium citrate as an anticoagulant. This avoided the hazards of clotting in the interval between drawing and administering blood and yet permitted the observance of aseptic precautions. The procedure was much simpler than the direct methods which required surgical teams and operating room technic.The citrate method came into favor very slowly. Early apparatus described by Hoffman (10) and Brines (11) involved suction for collecting and positive air pressure for injecting. Reactions were common. A review of transfusion procedure by Herr as late as 1925 (12) indicated that the direct was still preferred to the citrate method.The first successful preservation of human whole blood was accomplished in 1916 by Rous and Turner (13) by the addition of dextrose to a sodium citrate anticoagulant. This solution was