Catalog Number 9734302 |
Device Problems
Device Reprocessing Problem (1091); Complete Blockage (1094)
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Patient Problem
No Patient Involvement (2645)
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Event Date 03/14/2014 |
Event Type
malfunction
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Manufacturer Narrative
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Lot # and manufacture date provided.The site does not wish to replace or return the tap.
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Manufacturer Narrative
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No patient information provided as no patient was involved in this concern.Device lot number, or serial number, not available at time of this report.Device manufacturing date is dependent on lot number/serial number, therefore, unavailable at this time.No parts have been received by the manufacturer.
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Event Description
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A medtronic representative reported that, the site is having difficulty removing bone from the tap instrument.There was no patient present when this issue was identified.
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Manufacturer Narrative
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Correction: on 13-oct-2015, it was noticed that a previous mdr submission contained incorrect information with regards to the common device name, product code and/or pma/510(k).This mdr is being submitted to correct this information.There is no new information to change the patient information, event description or manufacturer narrative that was previously reported.
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Search Alerts/Recalls
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