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Several selective media were evaluated for their suitability for the isolation and quantification of mesophilic Aeromonasspecies from naturally polluted samples. Satisfactory recoveries were obtained with most of them but only when densities of background microflora were low. When analysed samples were from highly polluted waters, results were inconsistent because they did not give quantitative recovery of mesophilic aeromonads or they did not permit ready differentiation of Aeromonasspecies from the competitive bacteria. A new medium was developed on the basis of the combination of some positive aspects of several published media, pril‐ampicillin‐dextrin‐ethanol (PADE) agar. The medium employs dextrin (Merck 3006) as a fermentable carbohydrate and pril, ampicillin and ethanol as inhibitory substances. Recovery on PADE agar from suspensions of 15 tested strains of Aeromonasprepared from pure cultures was excellent. The confirmation rate of typical colonies designated Aeromonasspp. isolated from polluted samples exceeded 90%. Recoveries of stressed aeromonad strains on both PADE agar and a non‐selective medium (TSA) did not show any significant difference (P0.05). PADE agar was more reliable for quantitative recovery of mesophilic aeromonads than the other selective media because of its characteristics: (i) inhibition of the swarming of Proteus, (ii) good reduction of the background, (iii) inhibition of the over growth of Klebsiellaspp., (iv) absence of NaCl makes it unfavourable for the growth of halophilic vibrios, (v) combination of two pH indicators permitted a very easy differentiation between Aeromonascolonies and the competitive microflora. The medium can also be used for isolation of aeromonads from various sources by membrane filtration.