EEOICPA CIRCULAR NO. 11-08 May 29, 2011
SUBJECT: Vitro Manufacturing SEC Class from January 1, 1958 through December 31, 1959.
The purpose of this Circular is to notify all Division of Energy Employees Occupational Illness Compensation (DEEOIC) staff of the new SEC class designation for the Vitro Manufacturing facility, in Canonsburg, Pennsylvania.
Pursuant to the Energy Employees Occupational Illness Compensation Program Act of 2000 (EEOICPA) and 42 C.F.R. Part 83, a petition was filed on behalf of workers from the Vitro Manufacturing facility in Canonsburg, Pennsylvania, to be added to the Special Exposure Cohort (SEC).
The decision to initiate this petition occurred after the National Institute for Occupational Safety and Health (NIOSH) determined that it could not reconstruct a dose under 42 C.F.R. § 83.13. NIOSH submitted its findings to the Advisory Board on Radiation and Worker Health (“the Board”). On March 30, 2011, the Board submitted recommendations to the Secretary of Health and Human Services (HHS) to add to the SEC an additional class of employees who worked at the Vitro Manufacturing facility, in Canonsburg, Pennsylvania.
On April 29, 2011, the Secretary of HHS designated the following class for addition to the SEC in a report to Congress:
All Atomic Weapons Employer employees who worked at Vitro Manufacturing in Canonsburg, Pennsylvania, from January 1, 1958 through December 31, 1959, for a number of work days aggregating at least 250 work days, occurring either solely under this employment, or in combination with work days within the parameters established for one or more other classes of employees included in the Special Exposure Cohort.
A copy of the Secretary’s letter to Congress recommending the designation is included as Attachment 1. Although Congress had the authority to reject the recommendation within a 30-day time frame, Congress took no action. Therefore, the SEC designation for this class became effective as of May 29, 2011, which was 30 days after the Secretary of HHS designated the class for addition to the SEC in the report to Congress.
This is the second SEC class in effect for Vitro Manufacturing. The previous class was the subject of DEEOIC Bulletin 09-08. To qualify under this SEC class, the employee must be an Atomic Weapons Employee who has worked at least 250 days at the Vitro Manufacturing facility, in Canonsburg, Pennsylvania, from January 1, 1958 through December 31, 1959. If the employee does not have 250 workdays at Vitro Manufacturing during the period of the class, the case file must be reviewed to determine if additional workdays in the SEC can be found by combining workdays from employment meeting the criteria for other SEC classes and aggregating them together to meet the 250 workday requirement.
While a new SEC class has been added for employees at the Vitro Manufacturing facility, NIOSH intends to use any internal and external monitoring data that may become available for an individual claim (and that can be interpreted using existing NIOSH dose reconstruction processes or procedures). Additionally, NIOSH can reconstruct internal and external dose for uranium extraction operations based upon source term information and can estimate occupational medical dose. This means that for claims that do not satisfy the SEC membership criteria, a partial dose reconstruction is to be performed by NIOSH.
A copy of the NIOSH letter to affected Vitro Manufacturing employees is included as Attachment 2.
This Circular should be used in conjunction with EEOICPA Bulletin 11-07, Special Exposure Cohort Claim Processing. A screening worksheet is included as Attachment 3.
The reason code “C08, - Rvwd per Circular 11-08” has been added to ECMS to be used in conjunction with the NA, ISL, ISU, ISD, SER, and SEF codes as outlined in EEOICPA Bulletin 11-07.
RACHEL P. LEITON
Director, Division of Energy Employees
Occupational Illness Compensation
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