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FDA Breast Implant Recall ~ Dr Greer Explains the Recall
Dr. Greer is Board Certified by the American Board of Plastic Surgery. Greer Plastic Surgery cares for patients in the greater Cleveland area, and Dr. Greer operates at the Lake Health Hospital System. She currently serves as the chair of the Ethics Committee for the Lake Hospital System.
Board Certification – Plastic and Reconstructive surgery Education

University of Chicago, BA Biological Sciences
Case Western Reserve University, Master’s Degree in Bioethics
Case Western Reserve University, Medical Degree
Saint Louis University, Residency in Plastic Surgery

The FDA requested that Allergan recall all BIOCELL textured breast implants and tissue expanders marketed in the U.S. based on newly submitted Medical Device Reports (MDRs) reporting worldwide cases of BIA-ALCL and BIA-ALCL-related deaths associated with these devices. Allergan has notified the FDA that it will recall its BIOCELL textured breast implants and tissue expanders from the global market.

These products have the same BIOCELL textured surface (shell), which is a unique surface used only by Allergan. A list of Allergan's BIOCELL textured devices marketed in the U.S. that will be voluntarily recalled can be found at the end of this communication.
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