Novant Health Rowan Family Physicians

CLIA Laboratory Citation Details

3
Total Citations
7
Total Deficiencyies
6
Unique D-Tags
CMS Certification Number 34D0243593
Address 650 Julian Road, Salisbury, NC, 28147
City Salisbury
State NC
Zip Code28147
Phone704 637-3373
Lab DirectorRONALD BARRIER

Citation History (3 surveys)

Survey - January 6, 2026

Survey Type: null

Survey Event ID: CQ9U11

Deficiency Tags: D2130 D6016 D2016 D6000

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 2025 API (American Proficiency Institute) proficiency testing results, the laboratory failed to successfully participate in proficiency testing for the analyte WBC Diff (White Blood Cell Differential) for 2 of 3 consecutive testing events in 2025. Refer to 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 -- (f) 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 2025 API proficiency testing results, the laboratory failed to achieve satisfactory performance for WBC Diff on 2 of 3 consecutive testing events, resulting in unsuccessful performance. Findings: 1. Review of the CMS Casper reports revealed the following scores: a. 2025 Event 1 = 24% b. 2025 Event 3 = 0% 2. Review of the API proficiency testing results for these events confirmed the above scores. 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 2025 API proficiency testing results, the laboratory director failed to provide overall management and direction to ensure successful proficiency testing participation. Refer to D6016. D6016 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1407(e)(4)(i) (e)(4)(i) 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 2025 API proficiency testing results, the laboratory director failed to ensure successful participation in proficiency testing as required in Subpart H. Refer to D2130. -- 2 of 2 --

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Survey - August 14, 2025

Survey Type: Standard

Survey Event ID: 0OC811

Deficiency Tags: D6054

Summary:

Summary Statement of Deficiencies D6054 TECHNICAL CONSULTANT RESPONSIBILITIES CFR(s): 493.1413(b)(9) (b)(9) Thereafter, evaluations must be performed at least annually This STANDARD is not met as evidenced by: Based on review of technical consultant (TC) delegation of responsibilities, review of 2022, 2023, 2024 and 2025 testing personnel (TP) competency assessment records and interview with TC 08/14/25, the TC failed to perform annual competencies for 1 of 3 TP for the Urine Microalbumin/Creatinine ratio (ACR), Creatine Kinase-MB (CKMB), Troponin (TROP), Myoglobin (Mb) and D-Dimer testing from December of 2022 until May of 2025, a period of approximately 29 months. Findings: Review of TC delegation of responsibilities revealed under Section 4 "...Evaluating the competency of all testing personnel and assuring that the staff maintain their competency to perform test procedures and report test results promptly, accurately and proficiently.". Review of 2022, 2023, 2024 and 2025 TP #2 competency assessment records revealed the TC evaluated competency of TP #2 in December of 2022 for the ACR, CKMB, TROP, Mb, and D-Dimer testing. The next evaluation of competency was performed in May of 2025, a period of approximately 29 months later. Interview with TC at approximately 12:00 p.m. confirmed the competency assessments for TP #2 were not performed annually as required. They stated TP #2 was not available during the times the TC was on-site to perform competency assessments. 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 --

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Survey - December 17, 2019

Survey Type: Standard

Survey Event ID: EXSO11

Deficiency Tags: D5417 D5417

Summary:

Summary Statement of Deficiencies D5417 TEST SYSTEMS, EQUIPMENT, INSTRUMENTS, REAGENT CFR(s): 493.1252(d) Reagents, solutions, culture media, control materials, calibration materials, and other supplies must not be used when they have exceeded their expiration date, have deteriorated, or are of substandard quality. This STANDARD is not met as evidenced by: Based on observation and interview with TC (technical consultant) on 12/17/2019, the laboratory failed to discard vacutainer blood tubes that had exceeded their expiration dates. Findings: During tour of the laboratory at approximately 3 pm, the surveyor observed expired light blue Sodium (NA) Citrate vacutainer blood tubes (lot #9004633, expiration date: 10/31/19) located in drawing area #2 and clinical area "Hall A", that were available for use. During interview at approximately 3:05 pm, the TC confirmed the vacutainer tubes were expired. She stated the laboratory does not send out light blue NA Citrate tubes for testing very often. 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 --

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