This complaint is in scope of a complaint remediation project and has been identified as a complaint that required a mdr based on either the source of the complaint or the type of complaint and is being reported.This report is being submitted in pursuant to the provisions of 21 cfr, part 803.This report does not reflect a conclusion by anika or its employees that the report constitutes an admission that the device, anika, or its employees caused or contributed to a potential patient event documented on this report.On 15august2019 anika received from the fda a medwatch report (mw5088344) which reported off label use of orthovisc for osteoarthritis of the left ankle of a patient of unknown age and demographics.The lot number was not provided.There was no negative patient impact reported.There was no malfunction reported.
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