Clove (Syzygium aromaticum (L.) Merr. & Perry) is grown worldwide for its aromatic flower buds, which are used as a spice and pharmaceutical ingredient. It is a large tree that can reach 15 m in height and live for over 100 years. In 2017, the disease was observed in clove plantations in northeastern Brazil, lower south region of Bahia State (13°21′27.11″S 39°8′25.19″E). Observed tree losses ranged from 10% on some farms to 90% on others. This region is the main clove producing area of Brazil. The losses were attributed to “sudden death,” first reported by Nutman and Roberts (1953) to be devastating clove plantations in the Zanzibar Archipelago of Tanzania. There, the causal agent was identified as Valsa eugeniae Nutman & Roberts, which was renamed Cytospora eugeniae (Nutman & F.M. Roberts) G. C. Adams & Rossman (Rossman et al. 2015). In Brazil, as in Tanzania, symptom progression on affected trees consisted of a sudden shedding of green leaves and wilting of the remaining leaves, which acquired a reddish-brown color while still in the tree. Concurrent with defoliation, the young roots on affected trees exhibited decay, and the wood just under the bark on tree trunks developed an intense yellow color. Canopy symptoms (rapid or delayed leaf fall) varied, depending on air humidity during disease onset. On the affected clove trees in Brazil, we observed ascostromata (n = 30) typical of C. eugeniae immersed in the bark, valsoid, with black perithecia commonly in groups of 4 to 12, occasionally found alone or in groups of 50 or more. Perithecia globose, 240 to 335 µm, with long ostioles of 600 to 4,000 µm (n = 50) above surfaces; asci sessile, unitunicate, subclavate, apex rounded, 8-spored, 16 to 21 (19) × 3.6 to 5.7 (4.5) µm (n = 50); ascospores hyaline, allantoid, aseptate, 4.5 to 6.3 (5.2) × 1.4 to 2.2 (1.9) µm (n = 50). We isolated C. eugeniae from symptomatic stem and root fragments, collected from clove trees affected by sudden death. The tissue pieces, surface sterilized and rinsed in sterile water, were cultured on PDA and incubated at 25°C with a 12-h photoperiod. Subcultures of the fungus on PDA produced pycnidia dark, unilocular, globose or ovoid, 250 to 330 µm in diameter (n = 50); conidiophores hyaline, branched, 10 to 40 × 1 to 2 µm; conidiogenous cells enteroblastic, phialidic, 7 to 18 × 1 to 1.8 µm; conidia hyaline, allantoid, aseptate, 2 to 4 (3.1) × 0.7 to 1.6 (1.1) µm. Morphological identification was confirmed by DNA sequencing. The DNA was extracted from pure culture and ITS sequences were obtained using ITS1/ITS4 primers (White et al. 1990). The sequence obtained (527 bp) (GenBank MN460826) was 100% similar to C. eugeniae (KY051813, KY051811, KY051810). For inoculation tests, a 20 µl aliquot of a suspension of six isolates from pathogen (10⁶ conidia/ml) was pipetted on a wound (1 cm long) made with a knife in the bark of clove stem fragments (20 cm long, 2 to 4 cm diam.). Distilled water only and non-pathogen fungus (Phomopsis sp.) were used as negative controls. The fragments were incubated in a humid chamber at 25°C. Each treatment was replicated six times. Fifteen days after inoculation, all isolates produced lesions on the inoculated fragments (mean infected area 15.33 cm²), while controls showed no symptoms. Cultures reisolated from lesions exhibited morphological characteristics identical to those of C. eugeniae. To our knowledge, this is the first report of C. eugeniae causing sudden death disease in Brazil. Elucidation of the cause of sudden death may provide a foundation for development of management strategies for the disease.