FDA Adverse Event Injury Summary report: N

L-HOOK TIP

MDR report key: 4059 · Received July 9, 1992

Report

Report Number
4059
Event Type
Injury
Date Received
July 9, 1992
Date of Event
May 13, 1992
Report Date
June 2, 1992
Manufacturer
DAVOL
Product Code
KCH
Adverse Event
Yes
Report Source
User Facility report

Narratives

Description of Event or Problem · 1

ON 5/13/92, DURING A LAPARASCOPIC CHOLESCYSTECTOMY, THE L-HOOK TIP DEVICE WAS LAID ON THE SURGICAL DRAPES COVERING THE PATIENT BETWEEN USE OF THE L-HOOK TIP AND THE ENDO-FLO SUCTION/IRRIGATION PROBE. AT THE END OF THE OPERATIVE PROCEDURE, A BLACK SPOT WAS NOTICED ON THE DRAPE COVERING THE PATIENT'S MOUTH. UPON REMOVAL OF THE DRAPES, THE PATIENT WAS NOTED TO HAVE A SECOND DEGREE BURN ON THE UPPER LIP. THE PATIENT IS BEING FOLLOWED AS AN OUTPATIENT BY HER SURGEON AND A PLASTIC SURGEON. THE OPERATING ROOM STAFF NOW USES A MAYO STAND OVER THE PATIENT TO HOLD SUCH DEVICES WHERE NO HOLSTER OR CADDY IS PROVIDED FOR THE DEVICE. THE DEVICE WAS ON TRAIL USE IN OUR OPERATING ROOM AT THE TIME OF THE OCCURRENCE.INVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE. PATIENT MEDICAL STATUS PRIOR TO EVENT: SATISFACTORY CONDITION. THERE WAS NOT MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY. NO IMMINENT HAZARD TO PUBLIC HEALTH CLAIMED. DEVICE USED AS LABELED/INTENDED.INVALID DATA - REGARDING EVALUATION BY USER AFTER EVENT. METHOD OF EVALUATION: INVALID DATA. RESULTS OF EVALUATION: INVALID DATA. CONCLUSION: INVALID DATA. CERTAINTY OF DEVICE AS CAUSE OF OR CONTRIBUTOR TO EVENT: INVALID DATA. CORRECTIVE ACTIONS: DEVICE TEMPORARILY REMOVED FROM SERVICE. THE DEVICE WAS NOT DESTROYED/DISPOSED OF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 L-HOOK TIP KCH DAVOL

Patients

Seq Age Sex Outcome Treatment
1 40 YR Required Intervention