Since its U.S. launch in 2002, a unique product developed by Medtronic to promote bone growth has been used to mend the ailing backs of thousands of patients and has reaped millions for the Fridley med-tech giant -- a true blockbuster.
But on Tuesday, Medtronic revealed that the U.S. Justice Department is investigating how the product, called Infuse, is being used "off-label" in ways not vetted for safety and effectiveness by the Food and Drug Administration (FDA).
The company said it is complying with a Justice Department subpoena but declined to comment further or provide a copy of the document.
The subpoena is the latest of several inquiries to swirl around Medtronic and certain marketing practices in its high-flying spine business. At issue are Medtronic's payments to influential surgeons who are in a position to use and promote its products. Medtronic has denied claims in two federal whistle-blower lawsuits and says its payments to doctors are legal and proper ways to compensate physicians for their time and expertise.
Promotion at issue
Off-label use of Infuse prompted a 2007 whistle-blower lawsuit against a number of the nation's top spine surgeons, including nine in the Twin Cities, claiming that Medtronic promoted unapproved use of the product by paying doctors thousands of dollars in kickbacks. The doctors have all denied the charges.
Infuse, part of a successful spinal business that now represents 22 percent of Medtronic's revenue, was initially approved for use in the lower back. But many doctors have used it in the neck, occasionally with disastrous results.
In July, the FDA warned doctors that it has received 38 reports of complications in the past four years associated with the use of Infuse to repair the cervical spine.