Device was used for treatment, not diagnosis.(b)(4).Device is not expected to be returned for manufacturer review/investigation device evaluation/investigation could not be completed; no conclusion could be drawn as product was not returned to manufacturer.Device history records review could not be completed without lot number.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.This is one of three medwatches being submitted as three devices were involved in this event.See medwatch 2214133-2019-00100, 2214133-2019-00101& 2214133-2019-00102.The same consumer is represented in each medwatch.
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