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DuPont VP Who Oversaw Internal PFAS Toxicity Studies
DuPont Vice President of Safety, Health and Environmental Affairs who oversaw the company's internal toxicology studies on PFAS chemicals, including perfluorooctanoic acid (PFOA/C8), while the company concealed evidence of harm from regulators and the public for decades
Dr. Bruce Karrh served as DuPont's Vice President of Safety, Health and Environmental Affairs from the late 1970s through the 1990s, a period during which DuPont conducted extensive internal toxicology studies on perfluorooctanoic acid (PFOA, also known as C8), a synthetic chemical used in the production of Teflon and other fluoropolymer products at DuPont's Washington Works plant near Parkersburg, West Virginia. Under Karrh's oversight, DuPont's internal research documented serious health effects from PFOA exposure as early as the 1960s and 1970s. Company scientists found that PFOA accumulated in workers' blood, caused liver damage in animal studies, and was linked to birth defects in children of female workers at the Washington Works facility. A 1981 internal DuPont study found that two of seven children born to women working in the Teflon division had birth defects, including one with eye and tear duct deformities consistent with PFOA exposure seen in animal studies. Despite these findings, DuPont did not disclose the results to workers or regulators. Karrh, as the senior executive responsible for environmental and health affairs, was in a position to know about and acted on these internal studies. Internal company documents later revealed in litigation showed that DuPont's corporate medical department under Karrh's purview tracked worker blood PFOA levels and knew the chemical was bioaccumulating in employees and in the water supply surrounding the Parkersburg plant. By the mid-1980s, DuPont knew that PFOA had contaminated the drinking water of tens of thousands of residents in the mid-Ohio Valley. Rather than disclose the contamination, the company continued production and disposed of PFOA-laden waste in unlined landfills and directly into the Ohio River. The C8 Science Panel, an independent epidemiological study panel created as part of a 2005 class-action settlement, later found probable links between PFOA exposure and six diseases: kidney cancer, testicular cancer, thyroid disease, ulcerative colitis, high cholesterol, and pregnancy-induced hypertension. DuPont ultimately faced thousands of personal injury lawsuits and paid hundreds of millions in settlements. The EPA fined DuPont $16.5 million in 2005 for failing to report PFOA health risks under the Toxic Substances Control Act (TSCA) Section 8(e), which requires companies to report substantial risk information to the EPA. It was the largest civil administrative penalty the EPA had ever assessed at the time.
Oversaw DuPont's internal toxicology program during the decades when company scientists documented that PFOA accumulated in workers' blood, caused liver damage in animal studies, and was linked to birth defects in children of female workers
A 1981 internal DuPont study found that two of seven children born to women working in the Teflon division had birth defects; the results were not disclosed to workers or regulators
DuPont's corporate medical department under his purview tracked worker blood PFOA levels and knew the chemical was bioaccumulating in employees and contaminating the drinking water of tens of thousands of mid-Ohio Valley residents
Despite knowing PFOA had contaminated local water supplies by the mid-1980s, DuPont continued production and waste disposal practices that spread the contamination
The EPA fined DuPont $16.5 million in 2005 for failing to report PFOA health risks as required under TSCA Section 8(e), the largest civil administrative penalty the EPA had assessed at that time
The C8 Science Panel later found probable links between PFOA exposure and six diseases: kidney cancer, testicular cancer, thyroid disease, ulcerative colitis, high cholesterol, and pregnancy-induced hypertension
Internal company documents revealed in litigation showed systematic concealment of PFOA health data from regulators, workers, and surrounding communities over a period spanning decades
DuPont CEO (1998-2009) who led the company during the period when PFOA contamination became public
DuPont CEO who inherited the PFAS contamination liability and oversaw the DowDuPont merger
4 documented sources from official records, investigations, and reports
1960s
DuPont begins internal toxicology studies on PFOA; early results show the chemical is toxic to animals and bioaccumulates in human blood
1979
Karrh assumes senior role in DuPont's Safety, Health and Environmental Affairs division
1981
Internal DuPont study finds two of seven children born to female Teflon division workers have birth defects; results are not disclosed to workers or regulators
1984
DuPont internal documents show the company knows PFOA has contaminated the drinking water supply of communities surrounding the Parkersburg, West Virginia plant
1991
DuPont sets an internal guideline of 1 part per billion for PFOA in drinking water but does not share this with the EPA or affected communities
2001
Farmer Wilbur Tennant and attorney Robert Bilott file a federal lawsuit against DuPont, beginning the legal process that will expose decades of internal PFOA research
2004
EPA files administrative complaint against DuPont for failure to report substantial risk information about PFOA under TSCA Section 8(e)
2005-12
EPA settles with DuPont for $16.5 million, the largest civil administrative penalty in EPA history at that time; DuPont also agrees to fund the independent C8 Science Panel study
2012
C8 Science Panel completes its seven-year study and finds probable links between PFOA exposure and kidney cancer, testicular cancer, thyroid disease, ulcerative colitis, high cholesterol, and pregnancy-induced hypertension