Understanding complex interactions in cellular systems requires accurate tracking of individual cells observed in microscopic image sequence and acquired from multi-day in vitro experiments. To be effective, methods must follow each cell through the whole experimental sequence to recognize significant phenotypic transitions, such as mitosis, chemotaxis, apoptosis, and cell/cell interactions, and to detect the effect of cell treatments. However, high accuracy long-range cell tracking is difficult because the collection and detection of cells in images is error-prone, and single error in a one frame can cause a tracked cell to be lost. Detection of cells is especially difficult when using bright field microscopy images wherein the contrast difference between the cells and the background is very low. This work introduces a new method that automatically identifies and then corrects tracking errors using a combination of combinatorial registration, flow constraints, and image segmentation repair.