Regional Medical Oncology Center

CLIA Laboratory Citation Details

3
Total Citations
8
Total Deficiencyies
7
Unique D-Tags
CMS Certification Number 34D2044957
Address 2624 Ortho Drive, Wilson, NC, 27893
City Wilson
State NC
Zip Code27893
Phone252 991-5261
Lab DirectorKEITH LERRO

Citation History (3 surveys)

Survey - May 8, 2025

Survey Type: Standard

Survey Event ID: 2PZK11

Deficiency Tags: D0000

Summary:

Summary Statement of Deficiencies D0000 The Regional Medical Oncology Center laboratory was found in compliance with 42 CFR Part 493 Requirements for Laboratories as a result of an on-site survey performed May 08, 2025. Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 1 --

πŸ”’ Unlock Deficiency Summary

Get full access to the detailed deficiency summary for this facility

One-time payment β€’ Lifetime access

Survey - March 5, 2024

Survey Type: Special

Survey Event ID: VTDE11

Deficiency Tags: D2016 D6000 D2130 D6016

Summary:

Summary Statement of Deficiencies D2016 SUCCESSFUL PARTICIPATION CFR(s): 493.803(a)(b)(c) (a) Each laboratory performing nonwaived testing must successfully participate in a proficiency testing program approved by CMS, if applicable, as described in subpart I of this part for each specialty, subspecialty, and analyte or test in which the laboratory is certified under CLIA. (b) Except as specified in paragraph (c) of this section, if a laboratory fails to participate successfully in proficiency testing for a given specialty, subspecialty, analyte or test, as defined in this section, or fails to take remedial action when an individual fails gynecologic cytology, CMS imposes sanctions, as specified in subpart R of this part. (c) If a laboratory fails to perform successfully in a CMS- approved proficiency testing program, for the initial unsuccessful performance, CMS may direct the laboratory to undertake training of its personnel or to obtain technical assistance, or both, rather than imposing alternative or principle sanctions except when one or more of the following conditions exists: (1) There is immediate jeopardy to patient health and safety. (2) The laboratory fails to provide CMS or a CMS agent with satisfactory evidence that it has taken steps to correct the problem identified by the unsuccessful proficiency testing performance. (3) The laboratory has a poor compliance history. This CONDITION is not met as evidenced by: Based on desk review of CMS (Centers for Medicare and Medicaid Services) Casper reports 153D and 155D and desk review of 2023 API (American Proficiency Institute) proficiency testing results 3/5/24, the laboratory failed to successfully participate in proficiency testing for WBC (white blood cell) Differential on two consecutive testing events. See the deficiency cited at D2130. D2130 HEMATOLOGY CFR(s): 493.851(f) Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 2 -- Failure to achieve satisfactory performance for the same analyte in two consecutive events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on desk review of CMS Casper reports 153D and 155D and desk review of 2023 API proficiency testing results 3/5/24, the laboratory failed to achieve satisfactory performance for WBC Differential on two consecutive testing events, resulting in unsuccessful performance. Findings: 1. Desk review of CMS Casper reports 153D and 155D and 2023 API proficiency testing results revealed the laboratory received a score of 33% for WBC Differential on the 2023 API Hematology /Coagulation 2nd event. 2. Desk review of CMS Casper reports 153D and 155D and 2023 API proficiency testing results revealed the laboratory received a score of 67% for WBC Differential on the 2023 API Hematology/Coagulation 3rd event. D6000 MODERATE COMPLEXITY LABORATORY DIRECTOR CFR(s): 493.1403 The laboratory must have a director who meets the qualification requirements of 493. 1405 of this subpart and provides overall management and direction in accordance with 493.1407 of this subpart. This CONDITION is not met as evidenced by: Based on desk review of CMS Casper reports 153D and 155D and desk review of 2023 API proficiency testing results 3/5/24, the laboratory director failed to provide overall management and direction to ensure successful proficiency testing participation. See the deficiency cited at D6016. D6016 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1407(e)(4)(i) The laboratory director is responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform test procedures, and record and report test results promptly, accurate, and proficiently and for assuring compliance with the applicable regulations. (e) The laboratory director must-- (e)(4)(i) Ensure that the proficiency testing samples are tested as required under Subpart H of this part; This STANDARD is not met as evidenced by: Based on desk review of CMS Casper reports 153D and 155D and desk review of 2023 API proficiency testing results 3/5/24, the laboratory director failed to ensure successful participation in proficiency testing as required in Subpart H. See the deficiency cited at D2130. -- 2 of 2 --

πŸ”’ Unlock Deficiency Summary

Get full access to the detailed deficiency summary for this facility

One-time payment β€’ Lifetime access

Survey - September 12, 2018

Survey Type: Standard

Survey Event ID: 482V11

Deficiency Tags: D6021 D6046 D6046

Summary:

Summary Statement of Deficiencies D6021 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1407(e)(5) The laboratory director is responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform test procedures, and record and report test results promptly, accurate, and proficiently and for assuring compliance with the applicable regulations. (e) The laboratory director must-- (e)(5) Ensure that quality assessment programs are established and maintained to assure the quality of laboratory services provided. This STANDARD is not met as evidenced by: Based on review of laboratory quality assessment policy, review of quality assessment records and testing personnel (TP) interview 9/12/18, the laboratory director failed to ensure that all aspects of the laboratory's established quality assessment program were maintained from time of last survey, 8/25/16, until August 2018; a period of approximately 24 months. Review of laboratory's quality assessment policy revealed the laboratory director had established a quality assessment program that included a "Quality Assurance Monitoring Schedule" and "Monthly QA reviews"..."to include .... QC review, including CQAP report, Maintenance logs review, Temp and humidity level logs review, Patient test management review (5 records/month) and Complaints /problems/

πŸ”’ Unlock Deficiency Summary

Get full access to the detailed deficiency summary for this facility

One-time payment β€’ Lifetime access