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Medtronic Infuse Adverse-Event Reporting Gaps Spotlighted

The Minneapolis-based Star Tribune says Medtronic failed to report more than 750 adverse events uncovered during a 2006-2008 chart review of Infuse patients. But the company struck back, saying the newspaper’s version omits key facts.

An April 10 report

in the Minneapolis Star Tribune said Medtronic PLC did not properly report adverse events during a 2006-2008 chart reviewof its Infuse biologic-based spinal bone-growth device. But Medtronic rebutted...

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