COLD KNIFE, STRAIGHT BLADE, 3/PKG K-SB

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 2011-02-03 for COLD KNIFE, STRAIGHT BLADE, 3/PKG K-SB manufactured by Gyrus Acmi, Inc.

Event Text Entries

[16370304] During a surgical procedure while using the elite cold knife straight blade, the blade broke off in the pt. The surgeon was able to retrieve the blade without harming the pt.
Patient Sequence No: 1, Text Type: D, B5


[16416967] Performance report, no device is being returned; therefore we cannot determine the failure mode of the reported incident. We will monitor the complaint database for further occurrences. If further info becomes available, gyrus (b)(4) will continue the investigation and update the agency accordingly.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3006159227-2011-00001
MDR Report Key1981377
Report Source06
Date Received2011-02-03
Date of Report2011-02-03
Date of Event2011-01-03
Date Facility Aware2011-01-04
Date Mfgr Received2011-01-04
Date Added to Maude2012-05-10
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 Location3
Manufacturer ContactTERRENCE SULLIVAN
Manufacturer Street136 TURNPIKE RD
Manufacturer CitySOUTHBOROUGH MA 01772
Manufacturer CountryUS
Manufacturer Postal01772
Manufacturer Phone5088042739
Manufacturer G1GYRUS ACMI, INC
Manufacturer StreetCARRETERA SALTILLO- ZACATECAS KM 4.5
Manufacturer CityLA ANGOSTURA,SALTILLO, COAHUIL CP 25000
Manufacturer CountryMX
Manufacturer Postal CodeCP 25000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOLD KNIFE, STRAIGHT BLADE, 3/PKG
Generic NameCOLD KNIFE, STRAIGHT BLADE, 3/PKG
Product CodeGDX
Date Received2011-02-03
Model NumberK-SB
Catalog NumberK-SB
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGYRUS ACMI, INC
Manufacturer AddressCARRETERA SALTILLO- ZACATECAS KM 4.5 LA ANGOSTURA, CP MX


Patients

Patient NumberTreatmentOutcomeDate
10 2011-02-03

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