FREEMAN-GORNEY RHYTIDECTOMY SCISSORS, SUR P-6835 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,08 report with the FDA on 2003-11-17 for FREEMAN-GORNEY RHYTIDECTOMY SCISSORS, SUR P-6835 * manufactured by Padgett Instruments, Inc..

Event Text Entries

[16477686] Bought 2 new padgett super cut scissors for face lift from the sales representative. Although the scissors are new they didn't cut properly. Additional information was received in 2003 that these instruments were in contact with patients although no injuries have been reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1910735-2003-00038
MDR Report Key496687
Report Source01,08
Date Received2003-11-17
Date of Report2003-11-17
Date Mfgr Received2003-10-16
Date Added to Maude2003-11-24
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 FDA3
Event Location0
Manufacturer ContactJENNA KARABAS
Manufacturer Street311C ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362236
Manufacturer G1PADGETT INSTRUMENTS
Manufacturer Street1520 GRAND STREET
Manufacturer CityKANSAS CITY MO 64108
Manufacturer CountryUS
Manufacturer Postal Code64108
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFREEMAN-GORNEY RHYTIDECTOMY SCISSORS, SUR
Generic NamePADGETT SCISSORS
Product CodeHRR
Date Received2003-11-17
Model NumberP-6835
Catalog Number*
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key485414
ManufacturerPADGETT INSTRUMENTS, INC.
Manufacturer Address1520 GRAND ST. KANSAS CITY MO 641081404 US
Baseline Brand NameFREEMAN-GORNEY RHYTIDECTOMY SUPERCUT SCISSORS
Baseline Catalog NoP-6835
Baseline Device FamilyPADGETT SCISSORS
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 2003-11-17

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