Below are excerpts from a Health Department report from an on-site inspection at Planned Parenthood in Warminster, PA. This is public information. Thanks to a long time pro-life prayer warrior and sidewalk counselor for bringing this report to light.
This report is the result of an unannounced onsite survey conducted on August 14, 2019, at Planned Parenthood Keystone – Warminster (PPKey – Warminster). It was determined the facility was not in compliance with the requirements of the Pennsylvania Department of Health’s Rules and Regulations for Ambulatory Care Facilities, Annex A, Title 28, Part IV, Subparts A and F, Chapters 551-573, November 1999.
Based on review of facility documents, medical records (MR) and staff interview (EMP), it was determined the facility failed to meet the minimum Medicare standard 416.47(b) Standard: Form and Content of Record for compliance, that is established by the facility’s accrediting organization by failing to ensure the name of the physician and dosage of medications administered for a paracervical block (regional anesthesia causing a loss of sensation in a region of the body which results from the injection of a local anesthetic on each side of the cervix) was documented for one of six surgical abortion medical records reviewed (MR6); failing to ensure the maximum recommended dose of Lidocaine (an anesthetic) was not exceeded when administered as a paracervical block for one of six surgical abortion medical records reviewed (MR10).
Click here to read full report from PA Department of Health, including plan of corrections and dates required for rectifications.