SINGLE USE ENDO CLIP ML Adverse Event — Report (MDR 10001)

Name: SINGLE USE ENDO CLIP ML Adverse Event — Report (MDR 10001)
Creator: DeviceEvents

SINGLE USE ENDO CLIP ML Adverse Event — Report (MDR 10001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SINGLE USE ENDO CLIP ML; Manufacturer: UNKNOWN; Report number: 10001.

Device	SINGLE USE ENDO CLIP ML
Manufacturer	UNKNOWN
Report number	10001
Product problem	*
Date received	1994-07-21
Narrative	A PATIENT UNDERWENT A LAPARASCOPIC CHOLECYSTECTOMY; PROCEDURE WAS UNEVENTFUL; ENDO CLIPS X2 WERE USED ON THE CYSTIC ARTERY; SURGICAL BED WAS DRY WHEN CLOSED. PATIENT BEGAN HAVING DECREASED BP, INCREASED PULSE IMMEDIATELY UPON ARRIVAL IN RECOVERY ROOM; FLUID CHALLENGE UNSUCCESSFUL SO WAS RETURNED TO OR AND LAPARASCOPIC EXAM DONE. ENDO CLIPS WERE MISSING AND COULD NOT BE LOCATED. ARTERY WAS AGAIN CL
Source	openFDA MAUDE (device adverse events)

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