10MM HYDRO-DISSECTION PROBE Adverse Event — Report (MDR 10002)

Name: 10MM HYDRO-DISSECTION PROBE Adverse Event — Report (MDR 10002)
Creator: DeviceEvents

10MM HYDRO-DISSECTION PROBE Adverse Event — Report (MDR 10002) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 10MM HYDRO-DISSECTION PROBE; Manufacturer: UNKNOWN; Report number: 10002.

Device	10MM HYDRO-DISSECTION PROBE
Manufacturer	UNKNOWN
Report number	10002
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; THE 10MM HYDRO-DISSECTION PROBE WAS USED DURING IRRIGATION; 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 CLIP
Source	openFDA MAUDE (device adverse events)

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