SURGICAL KNIFE HANDLE #3L LONG 8-3/8IN SU1403-002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2015-05-14 for SURGICAL KNIFE HANDLE #3L LONG 8-3/8IN SU1403-002 manufactured by Carefusion.

Event Text Entries

[5950625] Customer stated "the open heart or staff is saying they are having a hard time getting the knife blades off the 3l knife handle we got and one nurse got cut trying to get it off. I don? T think that they had any problem getting them on just trying to get them off. A nurse was cut trying to remove the blade off knife handle. The nurse required stitches. The procedure that took place was an open heart surgery(valve) on (b)(6) 2015. Another instrument was used to complete the procedure. The instrument was not inspected prior to the procedure. The instrument has never been repaired. The current condition of the nurse is "fine".
Patient Sequence No: 1, Text Type: D, B5


[13357560] (b)(4). Upon carefusion investigation/evaluation of device, a follow up emdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[33294615] (b)(4): the following was initially reported to carefusion:? The open heart or staff is saying they are having a hard time getting the knife blades off the 3l knife handle we got and one nurse got cut trying to get it off. I don? T think that they had any problem getting them on just trying to get them off. I was not sure if we should send them back in or what you wanted to do. I wanted to see what you think. " additional information was received from the customer on may 6, 2015. ? A nurse was cut trying to remove the blade off knife handle. The nurse required stitches. The procedure that took place was an open heart surgery(valve) on (b)(6) 2015. Another instrument was used to complete the procedure. The instrument was not inspected prior to the procedure. The instrument has never been repaired. The current condition of the nurse is "fine". The complaint samples were returned and an evaluation was performed. The instruments were manufactured in january of 2015. A performance test and analysis were done with the instruments and no irregularities were found. The handles with blades were inspected by the production team and they found that the blades were easy to insert and remove. A review of the carefusion complaint system was performed for this product over the last 2 years. There have been no other reported complaints for this instrument of any kind during this time period. The reported issue will continue to be trended and evaluated by carefusion. A review of the device history record (dhr) was performed for this lot number. There were no issues identified with the material or manufacturing process that would have contributed to the reported issue. Unfortunately, the exact root cause could not be determined for the issue you experienced. It is possible the incorrect blade had been used or the instrument was mishandled.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1423507-2015-00033
MDR Report Key4772668
Report Source06
Date Received2015-05-14
Date of Event2015-04-28
Date Mfgr Received2015-04-28
Date Added to Maude2015-05-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactJILL RITTORNO
Manufacturer Street75 NORTH FAIRWAY DRIVE
Manufacturer CityVERNON HILLS IL 60061
Manufacturer CountryUS
Manufacturer Postal60061
Manufacturer Phone8473628056
Manufacturer G1CAREFUSION 2200, INC
Manufacturer Street75 NORTH FAIRWAY DRIVE
Manufacturer CityVERNON HILLS 60061
Manufacturer CountryUS
Manufacturer Postal Code60061
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSURGICAL KNIFE HANDLE #3L LONG 8-3/8IN
Generic NameHANDLE, SCALPEL
Product CodeGDZ
Date Received2015-05-14
Model NumberSU1403-002
Lot NumberXRFX
OperatorNURSE
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION
Manufacturer Address75 NORTH FAIRWAY DRIVE VERNON HILLS IL 60061 US 60061


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-05-14

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