USE ELITE/USA SERIES 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 06,07 report with the FDA on 1999-09-15 for USE ELITE/USA SERIES DISPOSABLE ACTIVE CORD DAC manufactured by Circon Acmi.

Event Text Entries

[19496072] User facility reported that sparking occurred while using device. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1519132-1999-00069
MDR Report Key241333
Report Source06,07
Date Received1999-09-15
Date of Report1999-09-15
Date Mfgr Received1999-08-20
Device Manufacturer Date1999-02-01
Date Added to Maude1999-09-23
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
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUSE ELITE/USA SERIES DISPOSABLE ACTIVE CORD
Generic NameACTIVE CORD
Product CodeFFZ
Date Received1999-09-15
Returned To Mfg1999-08-20
Model NumberDAC
Catalog NumberDAC
Lot NumberBC (2/99)
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key233819
ManufacturerCIRCON ACMI
Manufacturer Address93 NORTH PLEASANT ST. 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 1999-09-15

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