IRIX-70

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2005-11-02 for IRIX-70 manufactured by Trophy Radiologie.

Event Text Entries

[505405] Notified that irix 70 scissor arm was cracking, then broke.
Patient Sequence No: 1, Text Type: D, B5


[7832301] The reported condition is attributed to a failure of the support arm. This condition was identified by the manufacturer in 1995 and corrective actions were instituted at that time. The device cited in this report is involved in recall.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8020825-2005-00010
MDR Report Key764892
Report Source05
Date Received2005-11-02
Date of Report2005-10-25
Date of Event2005-10-05
Date Mfgr Received2005-10-06
Device Manufacturer Date1996-04-01
Date Added to Maude2006-09-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactLINDA SPITZER
Manufacturer Street1765 THE EXCHANGE
Manufacturer CityATLANTA GA 30339
Manufacturer CountryUS
Manufacturer Postal30339
Manufacturer Phone6785898673
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberZ-1099/1101-5
Event Type3
Type of Report3

Device Details

Brand NameIRIX-70
Generic NameDENTAL X-RAY SYSTEM
Product CodeEAP
Date Received2005-11-02
Model NumberNA
Catalog NumberNA
Lot NumberNA
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key752746
ManufacturerTROPHY RADIOLOGIE
Manufacturer Address4 RUE F. PELLOUTIER MARNE LA VALLEE CROISSY-BEAUBOURG CEDEX 2 FR 77437


Patients

Patient NumberTreatmentOutcomeDate
10 2005-11-02

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