Williams v. Mid-America Conversion Services, LLC

CourtDistrict Court, S.D. Ohio
DecidedDecember 11, 2023
Docket2:22-cv-02052
StatusUnknown

This text of Williams v. Mid-America Conversion Services, LLC (Williams v. Mid-America Conversion Services, LLC) is published on Counsel Stack Legal Research, covering District Court, S.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Williams v. Mid-America Conversion Services, LLC, (S.D. Ohio 2023).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF OHIO EASTERN DIVISION

BROCK WILLIAMS,

Plaintiff,

v. Case No. 2:22-cv-2052

JUDGE EDMUND A. SARGUS, JR.

Magistrate Judge Chelsey M. Vascura

MID-AMERICA CONVERSION

SERVICES, LLC,

Defendant.

OPINION AND ORDER This matter is before the Court on Defendant Mid-America Conversion Services, LLC’s Motion for Summary Judgment. (Mot., ECF Nos. 18, 19.) Plaintiff Brock Williams opposed (Opp., ECF No. 22), and Mid-America replied (Reply, ECF No. 24). For the reasons below, the Court GRANTS Mid-America’s Motion for Summary Judgment. BACKGROUND I. Factual Background Mid-America manages around 800,000 tons of Depleted Uranium Hexaflouride (“DUF6”) at two conversion facilities at United States Department of Energy sites near Paducah, Kentucky and Piketon, Ohio. (Lindsay Decl., ECF No. 19-1, ¶ 2.) DUF is a radiological material and a byproduct of processing uranium for use in nuclear weapons and in the commercial nuclear industry. (Id. ¶ 3.) The conversion facilities safely store and convert more than 63,000 large cylinders of DUF6 byproduct into a more stable form that can be reused, stored, or disposed of. (Id. ¶ 4.) Between February 18, 2019 and February 24, 2021, Mr. Williams worked as a Health Safety Technician – Radiological (“Technician”) for Mid-America at its Piketon facility. (Williams Dep., ECF No. 19-3, PageID 307, 361.) A. Mr. Williams’s job duties as a Technician included radiation work. As a Technician, Mr. Williams was “responsible for monitoring radiation levels within

the facility and detecting contamination.” (Lindsay Decl. ¶ 7.) As part of his job duties, Mr. Williams was to: provide “radiological monitoring and job coverage support for all DUF6 operations and maintenance activities”; “[c]onduct radiological safety walk-downs and pre-job walk downs”; and “maintain[] performance tests and operate[] radiological monitoring equipment.” (Position Description, ECF No. 19-3, PageID 411.) Mr. Williams’s Position Description also made clear that the facility environmental working conditions included frequent “[r]adiation work.” (Id.) Supporting the DUF6 operations required Mr. Williams to work in the Radiological Material Area (“RMA”) of the facility where DUF6 was stored. (Position Description, PageID 411; Lindsay Dep., ECF No. 19-2, PageID 218–19.) Due the nature of the work at Mid-America,

all employees risked exposure to some level of radiation. (Lindsay Dep. PageID 199.) By working in the RMA, however, Mr. Williams was exposed to radiation levels higher than the rest of the facility. (Id.) B. Mr. Williams had surgery on his hand. On December 5, 2019, after he had been working for Mid-America for about ten months, Mr. Williams underwent surgery on his hand, which had been crushed at a previous job, leaving him with chronic pain. (Williams Dep. PageID 322.) Mid-America accommodated Mr. Williams’s surgery and subsequent recovery. (Id.) Mr. Williams kept working with accommodations related to no-lifting and no use of his right arm until the Covid-19 pandemic led Mid-America to suspend its operations. (Id. PageID 315.) Mid-America placed about 65% of its Piketon employees on paid leave, including Mr. Williams. (Lindsay Decl. ¶ 10.) Mr. Williams remained on paid leave from March 26, 2020 through August 16, 2020. (Id.) C. Mr. Williams received a spinal cord stimulator device to reduce chronic pain in his hand. While on pandemic leave, Mr. Williams participated in a medical trial for a temporary spinal cord stimulator device whose purpose was to reduce his chronic pain. (Williams Dep. PageID 314–15, 321–22.) The temporary device reduced his pain from a 10/10 to a 3/10, so Mr. Williams decided to have the device permanently implanted and attached to his vertebra. (Id.)So less than a month after he returned to work post-pandemic, on September 5, 2020, Mr. Williams

underwent another surgery to alleviate the his chronic pain. (Id. PageID 321–22, 417.) Following the surgery to permanently implant the spinal cord stimulator, on October 12, 2020, Mr. Williams returned to work with a two-week, 15-pound weightlifting restriction. (Id. PageID 323.) Mid-America accommodated this restriction. (Id.) D. Mr. Williams’s stimulator device experienced technical issues due to radiation exposure. Shortly after his return to work, Mr. Williams asked to be moved to a position that kept him away from radiation exposure. Mr. Williams’s stimulator device had randomly shut off at least once while at work, leaving him in extreme pain. (Williams Dep. PageID 323–24, 333.) On October 22, 2020, Mr. Williams wrote to Mid-America: I was informed by the company that issued my spinal cord stimulator that I will be required to turn off my stimulating device while at work due to the wear and tear that the radiation exposure will have on the device. This will cause me to lose the ability again to use my right hand due to severe pain. I will also be required to be on permanent work restriction. Are there any accomidations (sic) that the company could offer or jobs that could be performed that would keep me away from radiation exposure so my device doesn’t need to be turned off?

(Id. PageID 420.) E. Mid-America requested more information on acceptable levels of radiation. Mid-America asked for the acceptable radiation levels Mr. Williams’s stimulator device could tolerate. (Williams Dep. PageID 421.) Given that all employees in Mid-America’s facilities are exposed to some minimal level of radiation, Mid-America felt it necessary to understand what level of radiation, if any, Mr. Williams could be exposed to, in order to evaluate whether Mid-America had any positions available for Mr. Williams. (Lindsay Decl. PageID 187.) Mid-America asked for formal direction from Mr. Williams’s doctors. (Lindsay Dep. PageID 222–23.) On October 26, 2020, Mr. Williams forwarded Rob Lindsay, the Environmental Safety

and Health Manager at Mid-America, Guidelines that Boston Scientific had provided to him for his stimulator device. (Williams Dep. PageID 425–26.) Under “Precautions,” the Guidelines explained that “[t]he following medical therapies or procedures may turn stimulation off or may cause permanent damages to the Stimulator, particularly if used in close proximity to the device . . . radiation therapy (Any damage to the device by radiation may not be immediately detectable).” (Id. PageID 439–40.) The Guidelines further instructed “[e]very effort should be taken to keep fields, including current, radiation, or high-output ultrasonic beams, away from the IPG [Implantable Pulse Generator].” (Id. PageID 443.) The next day, Mr. Williams provided Mid-America with a note from his doctor, Dr. Hoyt: “[e]very effort should be taken to keep fields, including current/radiation/high intensity

output/Ultrasonic beams away from the [device].” (ECF No. 22-1, PageID 747.) Later, Dr. Hoyt stated “[a]fter further evaluation and talking with Boston scientific [Mr. Williams] found that he can’t have the stimulator turned on at the nuclear plant he works at.” (Id.) Mid-America informed Mr. Williams that it needed more information about the device’s radiation tolerance. (Williams Dep. PageID 464–65.) In the meantime, Mid-America placed Mr. Williams on light duty. (Id.) It offered this temporary accommodations to minimize Mr. Williams’s radiation exposure. (Lindsay Decl. PageID 187.) Mr. Williams accepted that

accommodation and continued to receive full-time pay. (Id.) In the following months, Mid-America sought to glean additional information from Mr. Williams’s treating physicians.1 On November 3, 2020, Mid-America sent a letter to Dr. Hoyt for more information on whether Mr. Williams’s limitations were temporary or permanent restrictions. (Lindsay Dep. PageID 212–13.) Before Dr. Hoyt could respond, Mr.

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Williams v. Mid-America Conversion Services, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/williams-v-mid-america-conversion-services-llc-ohsd-2023.