CIRCON ACMI DISPOSABLE ACTIVE CORD DAC

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 1998-07-08 for CIRCON ACMI DISPOSABLE ACTIVE CORD DAC manufactured by Circon Acmi.

Event Text Entries

[20934001] Sparking and smoking reportedly observed at connection between cautery cord and resectoscope.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1519132-1998-00049
MDR Report Key176572
Report Source06
Date Received1998-07-08
Date of Report1998-07-08
Date of Event1998-06-01
Date Mfgr Received1998-06-10
Device Manufacturer Date1997-05-01
Date Added to Maude1998-07-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA3
Report to FDA3
Event Location0
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCIRCON ACMI DISPOSABLE ACTIVE CORD
Generic NameACTIVE CORD
Product CodeFFZ
Date Received1998-07-08
Returned To Mfg1998-06-10
Model NumberDAC
Catalog NumberDAC
Lot NumberEA (5/97)
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key166897
ManufacturerCIRCON ACMI
Manufacturer Address93 NORTH PLEASANT STREET NORWALK OH 448570409 US
Baseline Brand NameDISPOSABLE ACTIVE CORD
Baseline Generic NameACTIVE CORD
Baseline Model NoDAC
Baseline Catalog NoDAC
Baseline IDNA
Baseline Device FamilyACTIVE CORD
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1998-07-08

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