μ‐Oxido‐bis[(hexaethyldimethyl‐2,2′‐bidipyrrinato)iron(III)] (1) crystallizes as a mixed dichloromethane/water solvate as black plates in the triclinic system, space group P\bar{1}, with a = 14.536(3), b = 16.194(3), c = 25.883(5) Å, α = 98.89(3)°, β = 91.28(3)°, γ = 90.56(3)°, and Z = 2. In the crystal structure two distinct solvates 1·CH2Cl2 and 1·H2O are present in equal ratio. In both cases the solvent is found in direct vicinity of the Fe–O–Fe subunit and is located within a binding pocket formed by the two helically distorted tetrapyrroles. Whereas the dichloromethane molecule is oriented within this pocket as a dipole with the positive end pointing towards the oxygen atom of the Fe–O–Fe subunit, the water molecule forms a hydrogen bond with this site, supported by additional weak interactions with adjacent N‐donor atoms.