Important Safety Alerts

Important Safety Alerts

Medical Device Safety Alert: InBios International ZIKV Detect IgM Capture ELISA

28 Dec 2016

The United States Food and Drug Administration (FDA) has issued a medical device safety alert concerning ZIKV Detect IgM Capture ELISA, manufactured by InBios International, Inc.

The FDA is alerting physicians who care for pregnant women meeting CDC Zika virus clinical criteria and/or CDC Zika virus epidemiological criteria, that the U.S. commercial testing facility, Laboratory Corporation of America (LabCorp), has reported some false positive results from the ZIKV Detect test.

Because confirmation tests may take a week to a month to complete, the FDA is issuing this alert so that health care providers and patients know about a higher likelihood of false positive results.

The FDA urges health care providers to be aware that:

The FDA urges health care providers to:

For details, please refer to the FDA website:
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm534538.htm

If you are in possession of the affected products, please contact your supplier for necessary actions.

Posted on 28 December 2016

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