ARTICULATING ARM FOR CEILING MOUNT SYSTEM 5787

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2002-02-14 for ARTICULATING ARM FOR CEILING MOUNT SYSTEM 5787 manufactured by E-z-em, Inc..

Event Text Entries

[20241046] Customer reported that the articulating arm broke causing the injector to fall to the floor. The broken arm was found by the ct technologist. The injector head was in okay condition and was remounted onto a floor stand provided by e-z-em.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2432460-2002-00003
MDR Report Key377488
Report Source05,06,07
Date Received2002-02-14
Date of Report2002-01-15
Date of Event2002-01-14
Date Facility Aware2002-01-14
Report Date2002-01-15
Date Reported to Mfgr2002-01-15
Date Mfgr Received2002-01-15
Device Manufacturer Date2001-01-01
Date Added to Maude2002-02-22
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
Manufacturer ContactJUDITH MERITZ, VP.
Manufacturer Street717 MAIN STREET
Manufacturer CityWESTBURY NY 11590
Manufacturer CountryUS
Manufacturer Postal11590
Manufacturer Phone8005444624
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARTICULATING ARM FOR CEILING MOUNT SYSTEM
Generic NameCT INJECTOR ACCESSORY
Product CodeFIH
Date Received2002-02-14
Model NumberNA
Catalog Number5787
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNO INFO
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key366551
ManufacturerE-Z-EM, INC.
Manufacturer Address113-117 MAGNOLIA AVE. WESTBURY NY 11590 US
Baseline Brand NameARTICULATING ARM FOR CEILING MOUNT SYSTEM
Baseline Generic NameCT INJECTOR ACCESSORY
Baseline Model NoNA
Baseline Catalog No5787
Baseline IDNA
Baseline Device FamilyACCESSORY FOR PERCUPUMP INJECTOR SYSTEM
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK864227
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2002-02-14

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