Mammography Facility Adverse Event and Action Report - February 26, 2019: MLK - Heritage Health Center
Background
As part of the Mammography Quality Standards Act (MQSA), Congress mandated there be annual reporting of adverse actions taken against mammography facilities. Congress stipulated that the report be made available to physicians and the general public and that it should include information that is useful in evaluating the performance of mammography facilities nationwide. In order to provide this information in the timeliest manner, we now post the following information in “real time,” as actions taken against mammography facilities are concluded:
As part of the Mammography Quality Standards Act (MQSA), Congress mandated there be annual reporting of adverse actions taken against mammography facilities. Congress stipulated that the report be made available to physicians and the general public and that it should include information that is useful in evaluating the performance of mammography facilities nationwide. In order to provide this information in the timeliest manner, we now post the following information in “real time,” as actions taken against mammography facilities are concluded:
Mammography Facility Against Which There Was An Adverse Action
The State of Wisconsin
Facility Name and Address:
MLK-Heritage Health Center
2555 North Martin Luther King, Jr., Dr.
Milwaukee, WI 53212
MLK-Heritage Health Center
2555 North Martin Luther King, Jr., Dr.
Milwaukee, WI 53212
Facility ID Number:
222886
222886
Adverse Event:
On June 14, 2018, The American College of Radiology (ACR) initiated an Additional Mammography Review (AMR) of mammograms performed by this facility due to deficiencies noted with the clinical images submitted during the accreditation renewal process.
On June 14, 2018, The American College of Radiology (ACR) initiated an Additional Mammography Review (AMR) of mammograms performed by this facility due to deficiencies noted with the clinical images submitted during the accreditation renewal process.
On October 03, 2018, the ACR notified the FDA and the facility that the AMR revealed serious deficiencies with clinical image quality and failed to meet the ACR’s clinical image evaluation criteria.
Action Taken:
Based on the failed AMR results, on October 16, 2018, the ACR revoked the facility’s mammography accreditation.
Based on the failed AMR results, on October 16, 2018, the ACR revoked the facility’s mammography accreditation.
Furthermore, on October 16, 2018, the FDA declared the facility’s MQSA certificate to be no longer in effect until such time as the facility’s accreditation is reinstated and the facility has complied with all the requirements of the FDA.
Corrective Action:
Based on the serious image quality deficiencies noted during the AMR, the FDA required the facility to perform a Patient and Referring Healthcare Provider Notification (PPN) to alert all at-risk patients and their providers of the mammography quality problems at the facility.
Based on the serious image quality deficiencies noted during the AMR, the FDA required the facility to perform a Patient and Referring Healthcare Provider Notification (PPN) to alert all at-risk patients and their providers of the mammography quality problems at the facility.
The facility successfully completed the PPN and was notified of such by the FDA on January 23, 2019.
Status of the Facility:
The facility is currently not performing mammography.
The facility is currently not performing mammography.
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