STABILIZED COLD KNIFE G-500

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 1996-10-22 for STABILIZED COLD KNIFE G-500 manufactured by Circon Acmi.

Event Text Entries

[15010689] Cold knife blade broke during procedure; part of broken blade not found; x-ray and cystoscopy procedures failed to find missing piece.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1519132-1996-00015
MDR Report Key45118
Report Source06
Date Received1996-10-22
Date of Report1996-09-26
Date of Event1996-03-19
Device Manufacturer Date1987-08-01
Date Added to Maude1996-10-30
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
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTABILIZED COLD KNIFE
Generic NameCOLD KNIFE
Product CodeEZO
Date Received1996-10-22
Returned To Mfg1996-09-26
Model NumberG-500
Catalog NumberG-500
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key46012
ManufacturerCIRCON ACMI
Manufacturer Address93 N PLEASANT ST NORWALK OH 448570409 US
Baseline Brand NameCLASSIC SERIES STABILIZED COLD KNIFE
Baseline Generic NameURETHROTOME
Baseline Model NoG500
Baseline Catalog NoG500
Baseline IDNA
Baseline Device FamilyCOLD KNIFE
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1996-10-22

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