ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55 HP054

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-09-07 for ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55 HP054 manufactured by Ethicon Endo-surgery, Inc. (cincinnati).

Event Text Entries

[37132160] (b)(4). Info not available, device not returned for analysis.
Patient Sequence No: 1, Text Type: N, H10


[37132161] It was reported that during the unknown procedure, the 4-40 stud broke on the handpiece. No pt consequence.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1527736-2004-02938
MDR Report Key5351760
Date Received2004-09-07
Date of Report2004-08-30
Date of Event2004-06-02
Date Mfgr Received2004-08-30
Date Added to Maude2016-01-07
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 Location3
Manufacturer ContactGARY LEBLANC
Manufacturer Street4545 CREEK RD.
Manufacturer CityCINCINNATI OH
Manufacturer CountryUS
Manufacturer Phone5133378582
Manufacturer G1ETHICON ENDO-SURGERY, INC. (INDEPENDENCIA)
Manufacturer StreetNLVD INDEPENDENCIA
Manufacturer CityJUAREZ CHIHUAHUA
Manufacturer CountryMX
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NameULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
Generic NameHANDPIECE
Product CodeHBD
Date Received2004-09-07
Model NumberNA
Catalog NumberHP054
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, INC. (CINCINNATI)
Manufacturer AddressCINCINNATI OH US


Patients

Patient NumberTreatmentOutcomeDate
10 2004-09-07

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