The mitotic spindle pulls duplicated chromosomes apart using microtubules and motor proteins, but how it maintains and re-establishes force balance under mechanical perturbation was unclear. Using laser ablation to sever spindles in fission yeast at various stages of mitosis, our work shows that the severed poles collapse back toward each other, powered by the minus-end-directed motors dynein (Dhc1) and kinesin-14 (Klp2), rather than by passive viscoelastic relaxation of the nuclear envelope as previously assumed. This active, motor-driven response lets the spindle rescue its geometry and resume elongation after damage, showing that molecular motors, not just passive mechanics, actively defend the spindle's structural integrity.