← DeviceEvents
HomeDevice Adverse Events

CUFF STITCH, 70 DEG. RIGHT Adverse Event — Malfunction (MDR 1219602-2008-00021)

CUFF STITCH, 70 DEG. RIGHT Adverse Event — Malfunction (MDR 1219602-2008-00021) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CUFF STITCH, 70 DEG. RIGHT; Generic name: CUFF STITCH; Manufacturer: SMITH & NEPHEW INC., ENDOSCOPY DIV..

DeviceCUFF STITCH, 70 DEG. RIGHT
Generic nameCUFF STITCH
ManufacturerSMITH & NEPHEW INC., ENDOSCOPY DIV.
Report number1219602-2008-00021
Event typeMalfunction
Product problemY
Date received2008-02-19
Report sourceUser facility, Company representation
NarrativeTIP OF THE INSTRUMENT BROKE OFF IN PATIENT. FOREIGN BODY WAS NOT RETRIEVED/COULD NOT BE FOUND. AN X-RAY WAS TAKEN AT THE TIME TO LOCATE THE BROKEN PIECE. AT THIS TIME, THERE IS NO ADDITIONAL SURGERY SCHEDULED TO REMOVE THE BROKEN PIECE.
SourceopenFDA MAUDE (device adverse events)

🔍 Search all device adverse events →