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UNKNOWN DRILL Adverse Event — Malfunction (MDR 1020279-2020-01389)

UNKNOWN DRILL Adverse Event — Malfunction (MDR 1020279-2020-01389) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN DRILL; Generic name: GUIDE, SURGICAL, INSTRUMENT; Manufacturer: SMITH & NEPHEW, INC..

DeviceUNKNOWN DRILL
Generic nameGUIDE, SURGICAL, INSTRUMENT
ManufacturerSMITH & NEPHEW, INC.
Report number1020279-2020-01389
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, USER F
NarrativeIT WAS REPORTED THAT DURING SURGERY, DRILL COLD WELD INSIDE OF A DRILL GUIDE. NO INJURY WAS REPORTED. IT IS UNKNOWN IF THERE WAS A DELAY OR HOW WAS THE PROCEDURE CONCLUDED.
SourceopenFDA MAUDE (device adverse events)

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