FUTURA SAFETY SCALPEL 680010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2006-02-03 for FUTURA SAFETY SCALPEL 680010 manufactured by Futura Medical Products (p) Ltd (owned By Hypoguard).

Event Text Entries

[20192423] A physical therapy tech was cut by a safety scalpel, due to blade not retracting all the way, after debriding a pts wound.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1832816-2006-00002
MDR Report Key673075
Report Source08
Date Received2006-02-03
Date of Report2006-01-10
Date of Event2006-01-02
Date Mfgr Received2006-01-10
Date Added to Maude2006-02-13
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 ContactBRUCE MACFARLANE
Manufacturer Street5182 W 76TH STREET
Manufacturer CityEDINA MN 55439
Manufacturer CountryUS
Manufacturer Postal55439
Manufacturer Phone9526463188
Manufacturer G1FUTURA MEDICAL PRODUCTS (P), LTD.
Manufacturer StreetPLOT#7 COCHIN SPECIAL ECONOMIC ZONE
Manufacturer CityKAKKANAD, KOCHI 682030
Manufacturer CountryIN
Manufacturer Postal Code682 030
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameFUTURA SAFETY SCALPEL
Generic NameSAFETY SCALPEL
Product CodeGDX
Date Received2006-02-03
Returned To Mfg2006-01-30
Model Number680010
Catalog Number680010
Lot Number0503/179
ID NumberNA
Device Expiration Date2006-04-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key662383
ManufacturerFUTURA MEDICAL PRODUCTS (P) LTD (OWNED BY HYPOGUARD)
Manufacturer Address* KAKKANAD IN
Baseline Brand NameFUTURA SAFETY SCALPEL
Baseline Generic NameSAFETY SCALPEL
Baseline Model No680010
Baseline Catalog No680010
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2006-02-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.