Injured by Regenerative Medicine Products or Gene Therapy Procedures?

Posted on May 19, 2021 in Personal Injury

The FDA is cracking down on cellular-based treatment by manufacturers, clinics, and doctors, and so are we. Regenerative medicine products that have not been FDA-approved may be unsafe and cause serious side effects and even death. For instance, some medical spas (medispas or medspas), medical practices, orthopedic clinics, regenerative medicine, dermatology, and even plastic medical practices use various stem cell therapies that are not FDA approved as used.  In addition, some have used non-FDA sanctioned micro-needling, vampire facelifts, joint injections, or adipose-derived stem cells for joint injections or other purposes.

The FDA announced it intends to exercise enforcement against the selling and non-approved use of cellular and gene therapy products that violate regulations. The crux of this enforcement is to pursue unscrupulous clinics through whatever means necessary.

If you believe you have been injured by one of these gene therapy procedures, you can contact us for a free consultation.  Gallagher & Kennedy is committed to going after egregious violations by clinics and practitioners when they have harmed patients.  We will take action against manufacturers and health care providers who are offering unapproved regenerative medicine therapies that have harmed patients.

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