Allied Physicians Group, Pllc

CLIA Laboratory Citation Details

2
Total Citations
14
Total Deficiencyies
7
Unique D-Tags
CMS Certification Number 33D0986124
Address 2 Teleport Drive, Suite 107, Staten Island, NY, 10311
City Staten Island
State NY
Zip Code10311
Phone(718) 980-5437

Citation History (2 surveys)

Survey - June 6, 2022

Survey Type: Special

Survey Event ID: MTZT11

Deficiency Tags: D2016 D2128 D2130 D2131 D6000 D6016 D2016 D2128 D2130 D2131 D6000 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 Proficiency Test (PT) desk review of the Center for Medicaid & Medicare Services (CMS) PT data reports and PT summary reports from American Proficiency Institute (API) PT program, the laboratory failed to participate successfully in CMS approved proficiency testing program, for the speciality Hematology and the test analyte's Red Blood Cell Count (RBC), and Hematocrit (Hct) The following scores were assigned: Speciality Hematology 2021 third event = 73% 2022 first event = 0% (failure to participate) RBC and Hct 2021 third event = 20% 2022 first event = 0% (failure to participate) This is considered unsuccessful PT performance. Refer to D2130 and D2131 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 -- D2128 HEMATOLOGY CFR(s): 493.851(e) (1) For any unsatisfactory analyte or test performance or testing event for reasons other than a failure to participate, the laboratory must undertake appropriate training and employ the technical assistance necessary to correct problems associated with a proficiency testing failure. (2) For any unacceptable analyte or testing event score, remedial action must be taken and documented, and the documentation must be maintained by the laboratory for two years from the date of participation in the proficiency testing event. This STANDARD is not met as evidenced by: Based on PT desk review of the CMS PT data reports and PT summary reports from API PT program, the laboratory failed to participate successfully in CMS approved proficiency testing program, for the test analyte's White Blood Cell Count (WBC), Cell Identification (Cell I.D.), Hemoglobin (Hgb) and Platelet Count. The following scores were assigned: 2022 first event = 0% (failure to participate) This is considered unsatisfactory PT performance. D2130 HEMATOLOGY CFR(s): 493.851(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 PT desk review of the CMS PT data reports and PT summary reports from API PT program, the laboratory failed to participate successfully in CMS approved proficiency testing program, for the test analyte's RBC and Hct. The following scores were assigned: 2021 third event = 20% 2022 first event = 0% (failure to participate) This is considered unsuccessful PT performance. D2131 HEMATOLOGY CFR(s): 493.851(g) Failure to achieve an overall testing event score of satisfactory performance for two consecutive testing events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on PT desk review of the CMS PT data reports and PT summary reports from API PT program, the laboratory failed to participate successfully in CMS approved proficiency testing program, for the speciality Hematology. The following scores were assigned: 2021 third event = 73% 2022 first event = 0% (failure to participate) This is considered unsuccessful PT performance. D6000 MODERATE COMPLEXITY LABORATORY DIRECTOR CFR(s): 493.1403 The laboratory must have a director who meets the qualification requirements of 493. -- 2 of 3 -- 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 PT desk review of the CMS PT data reports and API PT program records, the laboratory director failed to fulfill the laboratory director's responsibilities and ensure that the laboratory achieved a satisfactory performance and successfully participate in a PT program, approved by CMS, for the speciality Hematology and the test analyte's Cell I.D./WBC Diff., RBC,Hct, HgB, WBC and Platelets. Refer to 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 PT desk review of the CMS PT data reports and API PT program records, the laboratory director failed to fulfill the laboratory director's responsibilities and ensure that the laboratory achieved a satisfactory performance and successfully participate in a PT program, approved by CMS, for the speciality Hematology and the test analyte's Cell I.D./WBC Diff., RBC,Hct, HgB, WBC and Platelets. The following scores were assigned: Speciality Hematology 2021 third event = 73% 2022 first event = 0% (failure to participate) RBC and Hct 2021 third event = 20% 2022 first event = 0% (failure to participate) This is considered unsuccessful PT performance. WBC, Cell I.D., Hgb and Platelet Count. The following scores were assigned: 2022 first event = 0% (failure to participate) This is considered unsatisfactory PT performance. -- 3 of 3 --

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Survey - February 1, 2019

Survey Type: Standard

Survey Event ID: 9Z8211

Deficiency Tags: D1001 D1001

Summary:

Summary Statement of Deficiencies D1001 CERTIFICATE OF WAIVER TESTS CFR(s): 493.15(e) Laboratories eligible for a certificate of waiver must-- (1) Follow manufacturers' instructions for performing the test; and (2) Meet the requirements in subpart B, Certificate of Waiver, of this part. This STANDARD is not met as evidenced by: Based on surveyor's review of the laboratory's procedure manual, lack of waived testing records and an interview with the testing person, the laboratory failed to record the quality control results, lot numbers and expiration dates for the Sekisui OSOM Ultra Rapid Strep A and Influenza A & B tests kits, and Roche Chemstrip 10SG urine test strips. FINDINGS INCLUDED: 1. The testing person confirmed at approximately 10:30 AM on February 1, 2019 that the laboratory failed to record the lot numbers, expiration dates and quality control results for Sekisui OSOM Ultra Rapid Strep A and Influenza A & B tests kits. 2. Sekisui OSOM Ultra Rapid Strep A and Influenza A & B manufacturer requires external positive and negative controls (provided in the test kits) be performed and documented with each new lot number/shipment of test kits. Approximately 200 patient specimens were tested and reported for Rapid Strep A and 40 patients for Influenza A & B from October 2018 through the survey date. 3. The laboratory failed to retain a copy of the Roche Chemstrip 10SG packet insert, therefore, the surveyor was not able to determine the quality control requires of urine test strips. The laboratory did not record the lot numbers and expiration dates for the urine test vials. Approximately 250 patient specimens were tested and reported from October 2018 through the survey date. 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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