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Memphis Defense Depot

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Location 2028, Memphis Depot Parkway, Memphis, Tennessee, 38114, United States
Years of Operation 1942-1997

The Memphis Defense Depot opened in 1942 as a logistical support facility for the military during World War II. This site was also a storage facility for hazardous materials. The EPA placed the site on the National Priorities List during the 90’s, and the depot officially closed in 1997. It was then converted into the Memphis Depot Industrial Park, which recently sold.

Known Toxins

The following chart outlines the toxins associated with this military location and the potential effects of exposure.*

Toxin Potential Effects
Strong Good Limited
Arsenic Potential Effects Peripheral neuropathy, Hyperkeratosis/Hyperpigmentation, Diabetes ­ Type II, Coronary artery disease, peripheral vascular disease, atherosclerosis Steatosis (fatty liver), Skeletal malformations, Renal (kidney) cancer, Raynaud's phenomenon, Pneumonitis hypersensitivity, Neural tube defects/CNS malformations, Nasal septal perforation, Myocardial ischemia, Low birth weight/Small for Gestational Age, Hypertension, Hepatoportal Sclerosis, Fetotoxicity (Miscarriage/spontaneous abortion; stillbirth), Congenital malformations ­ general, Cirrhosis, Cardiomyopathy, Bladder cancer, Arrhythmias, Anemia ­ hemolytic, Alopecia, Adult­-Onset Leukemias Neurosthenia (Organic affective syndrome), Myelodysplastic syndrome, Metal fume fever, Immune suppression, Hepatocellular cancer (Liver cancer), Genito­urinary malformations (includes cryptorchidism, hypospadias), Cognitive impairment (includes impaired learning, impaired memory, and decreased attention span), Acute tubular necrosis
Dieldrin Potential Effects - Hormonal changes (levels of circulating sex hormones ­ FSH/LH, Inhibin, and/or estrogens, progesterones, and androgens) Uterine cancer, Thrombocytopenia, Psychiatric disturbances, Parkinson's disease/Movement disorders, Lymphoma non ­Hodgkin's, Hormonal changes (levels of circulating sex hormones ­ FSH/LH, Inhibin, and/or estrogens, progesterones, and androgens), Colo­rectal cancer, Cognitive impairment (includes impaired learning, impaired memory, and decreased attention span), Breast cancer, Adult­-Onset Leukemias
Perchloroethylene (PCE) Potential Effects - - -
Polychlorinated Byphenyls (PCBs) Potential Effects Thyroid disorders ­Hypothyroidism, Porphyria ­ toxic, Developmental Delay, Decreased I.Q../Mental retardation, Cirrhosis, Chloracne, Behavioral problems, ADD/ADHD, hyperactivity Peripheral neuropathy, Pancreatic cancer, Menstrual disorders, Lymphoma non ­Hodgkin's, Low birth weight/Small for Gestational Age, Immune suppression, Hepatocellular cancer (Liver cancer), Dyslipidemia, hypercholesterolemia, Delayed growth, Congenital malformation Cranio­ Facial, Cognitive impairment (includes impaired learning, impaired memory, and decreased attention span), Bronchitis ­ chronic, Acute hepatocellular injury (Hepatitis), Abnormal sperm (morphology, motility, and sperm count) Testicular cancer, Reduced Fertility ­ Female (infertility and subfertility), Parkinson's disease/Movement disorders, Hypoactivity, Hypertension, Hyperkeratosis/Hyperpigmentation, Hearing loss, Endometriosis, Diabetes ­ Type I, Breast cancer, Bone cancer/Ewings sarcoma, Altered time to sexual maturation (accelerated or delayed puberty), Altered sex ratio
Polynuclear Aromatic Hydrocarbons (PAHs) Potential Effects Scrotal cancer, Porphyria ­ toxic, Laryngeal cancer Skin cancer (non­melanoma), Renal (kidney) cancer, Prostate cancer, Photosensitivity, Pancreatic cancer, Nasopharyngeal/Sino­Nasal cancer, Lung cancer, Immune suppression, Esophageal cancer, Breast cancer, Bladder cancer Reduced Fertility Male (infertility and subfertility), Oral cancer, Melanoma, Early onset menopause, Coronary artery disease, peripheral vascular disease, atherosclerosis, Colo­rectal cancer, Bone cancer/Ewings sarcoma, Adult­-Onset Leukemias
Trichloroethylene (TCE) Potential Effects Acute hepatocellular injury (Hepatitis) Scleroderma, Renal (kidney) cancer, Psychiatric disturbances, Lymphoma non ­Hodgkin's, Hepatocellular cancer (Liver cancer), Fetotoxicity (Miscarriage/spontaneous abortion; stillbirth), Decreased Coordination/ Dysequilibrium, Cirrhosis, Childhood Leukemias, Cardiac congenital malformations, Autoimmune antibodies, positive ANA, Arrhythmias Trigeminal neuropathy, Testicular cancer, Systemic Lupus Erythematosus, Raynaud's phenomenon, Prostate cancer, Peripheral neuropathy, Pancreatitis, Pancreatic cancer, Oral clefts (cleft lip and palate), Neural tube defects/CNS malformations, Nephrotic syndrome, Multiple myeloma, Lung cancer, Low birth weight/Small for Gestational Age, Immune suppression, Hodgkin's Disease (lymphoma), Genito­urinary malformations (includes cryptorchidism, hypospadias), Cognitive impairment (includes impaired learning, impaired memory, and decreased attention span), Choanal atresia, Cervical cancer, Brain cancer ­adult, Adult­-Onset Leukemias, ADD/ADHD, hyperactivity, Acute tubular necrosis

If you were stationed at Memphis Defense Depot and later experienced adverse health effects, you may be eligible for compensation.

*Effects are according to the Center for Disease Control and Prevention’s Agency for Toxic Substances & Disease Registry unless otherwise noted.