Hackensack Meridian Urgent Care Plus, Pc

CLIA Laboratory Citation Details

2
Total Citations
21
Total Deficiencyies
11
Unique D-Tags
CMS Certification Number 31D2311701
Address 5 Marine View Plaza, Hoboken, NJ, 07030
City Hoboken
State NJ
Zip Code07030
Phone(848) 308-4612

Citation History (2 surveys)

Survey - October 10, 2025

Survey Type: Standard

Survey Event ID: PK6D11

Deficiency Tags: D5219 D5401 D5469 D5479 D5219 D5401 D5469 D5479 D5803 D5805 D5803 D5805

Summary:

Summary Statement of Deficiencies D5219 EVALUATION OF PROFICIENCY TESTING PERFORMANCE CFR(s): 493.1236(c)(2) (c)(2) Any test or procedure listed in subpart I of this part for which compatible proficiency testing samples are not offered by a CMS-approved proficiency testing program. This STANDARD is not met as evidenced by: Based on surveyor review of the American Association of Bioanalysts Medical Laboratory Evaluation (AAB-MLE) Proficiently Testing (PT) records and interview with the Techincal Consultant (TC) the Laboratory Director (LD) failed to ensure that the laboratory participated in an accurate split sample assessment for Hematology testing. from 9/26/24 to 10/10/25. The findings include: 1. A review of AAB-MLE PT events 3-2024, and 1,2,3-2025 revealed that the laboratory did not verify accuracy of the following analytes. a) Mean Corpuscular Volume (MCV) b) Mean Corpuscular Hemoglobin (MCH) c) Mean Corpuscular Hemoglobin Concentration (MCHC) d) Red Cell Distribution Width (RDW) e) Mean Platelet Volume (MPV) f) Granulocytes absolute (GRA#) g) Monocytes absolute (MON#) h) Lymphocytes Absolute (LYM#) 2. The TP confirmed on 10/10/25 at 11:00 am that the LD did not ensure the laboratory participated in an accurate split sample assessment for the above mentioned tests. D5401 PROCEDURE MANUAL CFR(s): 493.1251(a) (a) A written procedures manual for all tests, assays, and examinations performed by the laboratory must be available to, and followed by, laboratory personnel. Textbooks may supplement but not replace the laboratory's written procedures for testing or examining specimens. Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 3 -- This STANDARD is not met as evidenced by: Based on surveyor review of the Procedure Manual (PM), Quality Control (QC) and interview with the Techincal consultant (TC) the laboratory failed to have a

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Survey - July 16, 2025

Survey Type: Special

Survey Event ID: 3PR611

Deficiency Tags: D0000 D2016 D2130 D6000 D2016 D2130 D6000 D6016 D6016

Summary:

Summary Statement of Deficiencies D0000 A proficiency testing desk review survey was performed on July 16, 2025, the laboratory was found not in compliance with the following CONDITION LEVEL DEFICIENCIES D2016 - 42 C.F.R. 493.803 Condition: Successful participation [proficiency testing] D6000 - 42 C.F.R. 493.1403 Condition: Laboratories performing moderate complexity testing; laboratory director 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 an office review of the CASPER reports 153 and 155 and proficiency testing 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 -- provider reports, the laboratory failed to achieve 80% or more in two out of three events for Hematology for the analyte Hematocrite (HCT) with the American Association of Bioanalysts (AAB). Refer to D2130 D2130 HEMATOLOGY CFR(s): 493.851(f) (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 review of the CASPER 155 report and graded results from American Association of Bioanalysts (AAB). The laboratory failed to achieve satisfactory performance (80% or greater) for two consecutive events in the subspecialty Hematology for the analyte Hemoatocrite (HCT) resulting in initial unsuccessful performance. The findings include: 1) A review of the CASPER 155 report revealed the following. a) The laboratory scored 60% for HCT in event 1-2025. b) The laboratory scored 40% for HCT in event 2-2025. 2. A review of AAB graded results confirmed the laboratory failed two consecutive Proficiency Testing (PT) events. 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 review of the CASPER 155 report and graded results from American Association of Bioanalysts (AAB), the Laboratory Director (LD) failed to provide overall management and direction to laboratory personnel to ensure that the Proficiency Testing (PT) surveys are performed satisfactorily and in compliance with Clinical Laboratory Improvement Amendments (CLIA) regulations. The findings include: 1. The LD failed to ensure PT surveys are performed satisfactorily and in compliance with CLIA regulations. Cross refer 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 a review of the CASPER 155 report and graded results from Association of Bioanalysts (AAB), the Laboratory Director (LD) failed to ensure successful participation in a Department of Health and Human Services (DHHS) approved Proficiency Testing (PT) program for two consecutive PT events for the analyte Hematocrit (HCT), resulting in initial unsuccessful performance. Refer to D2130. -- 2 of 2 --

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