SEMI-RIDID SCISSORS GYS-5

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2002-01-22 for SEMI-RIDID SCISSORS GYS-5 manufactured by Circon Acmi.

Event Text Entries

[17112091] Smoke coming from working element.
Patient Sequence No: 1, Text Type: D, B5


[20511899] Scissors screw detached from blades during hysteroscopy.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1519132-2002-00006
MDR Report Key374440
Report Source06,07
Date Received2002-01-22
Date of Report2002-01-22
Date of Event2001-12-20
Date Facility Aware2001-12-26
Report Date2002-01-22
Date Mfgr Received2001-12-26
Date Added to Maude2002-01-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJOHN DELUCIA
Manufacturer Street492 OLD CONNECTICUT PATH
Manufacturer CityFRAMINGHAM MA 017014584
Manufacturer CountryUS
Manufacturer Postal017014584
Manufacturer Phone5088790640
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSEMI-RIDID SCISSORS
Generic Name500
Product CodeJOK
Date Received2002-01-22
Returned To Mfg2002-01-10
Model NumberGYS-5
Catalog NumberGYS-5
Lot NumberBD (2/2000)
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key363568
ManufacturerCIRCON ACMI
Manufacturer Address93 NORTH PLEASANT STREET NORWALK OH 448570409 US
Baseline Brand NameSLIMLINE SEMI-RIGID SCISSORS
Baseline Generic NameSLIMLINE SEMI-RIGID SCISSORS
Baseline Model NoGYS-5
Baseline Catalog NoGYS-5
Baseline Device FamilyG2120
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 2002-01-22

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