Radiation-Emitting Products

MQSA Alternative Standard #19: Correction Period When Components of the Sectra MicroDose L30 Full Field Digital Mammography Imaging System Fail Quality Control Tests

This alternative standard was approved and became effective on June 1, 2011. It has no time limit. It allows a 30-day period for corrective actions following the failure of specified quality control tests by the Sectra MicroDose L30 Full Field Digital mammography imaging system. The specified tests are equivalent to quality control tests for screen-film systems for which a 30-day correction period is already allowed. The alternative standard specifies the quality control tests whose failures require corrective action before the failing component is used again during patient examinations. This division makes it clear that when the test failure is related to the acquisition of images only, image acquisition must cease until the problem is corrected but image interpretation can continue. Similarly if the test failure is related to devices used for image interpretation, image acquisition can continue but image interpretation with the failed component must cease until the problem is corrected.

The original standard is 21 CFR 900.12(e)(8)(ii), which states:

21 CFR 900.12(e)(8): Use of test results

(ii) If the test results fall outside of the action limits, the source of the problem shall be identified and corrective actions shall be taken:

(A) Before any further examinations are performed or any films are processed using the component of the mammography system that failed any of the tests, described in paragraphs (e)(1), (e)(2), (e)(4)(i), (e)(4)(iii), (e)(5)(vi), (e)(6), or (e)(7) of this section;
(B) Within 30 days of the test date for all other tests described in paragraph (e) of this section. 

The approved alternative is:

21 CFR 900.12(e)(8): Use of test results.

(ii) If the test results for the Sectra MicroDose L30 Full Field Digital Mammography imaging system, fall outside the action limits, the source of the problem shall be identified and corrective actions shall be taken:

(A) If any of the quality control tests that evaluate the performance of the image acquisition system fail any of the following tests as defined in the Sectra MicroDose Mammography L30 Quality Control Procedures, the source of the problem shall be identified and corrective action shall be taken before any further examinations are performed using that component.:

(1) Daily quality control
(2) Full calibration
(3) Mammographic accreditation phantom test
(4) Contrast-to-noise ratio
(5) Spatial resolution
(6) AEC system: Breast thickness and exposure
(7) Image quality evaluation
(8) Quick calibration
(9) Display quality control test (AWS)
(10) Compression
(11) Missed tissue at chest wall

(B) Before any further mammographic images are processed, interpreted or printed using the component of the imaging system that failed any tests as specified by the manufacturer as defined in the Sectra MicroDose Mammography L30 Quality Control Procedures. Clinical imaging may be continued. If available, an alternative approved diagnostic device may be used for mammographic image interpretation:

(1) Printer quality control test
(2) Display quality control test (RWS)
(3) Viewing conditions

(C) If any of the following quality control tests that evaluate the performance of the X-ray unit or the exposure function or the diagnostic device used for mammographic image interpretation produce results that fall outside the action limits as specified by the Sectra MicroDose Mammography L30 Quality Control Procedures, the source of the problem shall be identified and corrective action shall be taken within thirty days of the test date. Clinical imaging and mammographic image interpretation may be continued during this period:

(1) Visual checklist
(2) Repeat analysis test
(3) Thickness indication
(4) X-ray tube output (air kerma)
(5) Air kerma reproducibility
(6) Half value layer
(7) AEC system: Density compensation
(8) Tube voltage
(9) Image field and x-ray field agreement

 

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