MDXG: Undisclosed Adverse Reaction Contradicts Product Safety Claims

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MiMedx boldly claims on its website that it has “distributed more than 1 million allografts to date with zero reported adverse reactions attributed to our products”. Yet, according to a lawsuit filed earlier this month, an Epifix patient suffered an adverse reaction so severe that she was left permanently maimed. Read More

MiMedx: Undisclosed Failed Inspections, Illegal Injections, and the FDA

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This report specifically exposes severe undisclosed manufacturing problems and contamination risks. Even though FDA investigators identified issues that “pose a significant risk to the recipient”, the company is marketing unapproved products produced by these facilities for risky experimental indications such as spinal injections. Unsuspecting patients are being defrauded through false advertisements used by dubious clinics to entice them into receiving the injections. Because these activities appear to put patients in danger, we believe the FDA has no choice but to immediately intervene. Read More

An Open Letter To MiMedx Director Luis Aguilar

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We are writing you to express our belief that the ongoing fraud at MiMedx must be stopped immediately and our opinion that you are uniquely positioned to do so.  You have an important opportunity to use your position as a MiMedx Director to protect your legacy and reputation. Read More

An Open Letter To The MiMedx Auditors

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We are writing to express our concerns about the risks of serious and pervasive fraud at Mimedx Group, Inc. and your firm’s audit thoroughly testing these risks in light of facts and allegations that have emerged. Read More