I would like to ask a counter question and that is in what way these globular substances interfering in your work. I feel that the presence of these globules should not matter much and hence I recommend not to spend time and energy trying to remove these. May be that time you can do some other good research work.
These are not globular objects but aggregates of agarose bound resins. You can change the pH and see no globular object will be there. Such artifacts appear only when you work in cold or near temperature of 4-8 0C.
A side note:it is possible to reuse beads, only if you recharge them. I usually reuse the beads and I haven't had any problem with it.Before recharging, i'd wash the beads with 500 mM imidazole to make sure that all proteins are removed from the beads.