SUPPORT ARM 177 6481720

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07 report with the FDA on 2013-11-04 for SUPPORT ARM 177 6481720 manufactured by Maquet Critical Care Ab.

Event Text Entries

[4055594] It was reported that the support arm broke. There was no pt involvement. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[11483943] The broken support arm has been requested back for investigation. A supplemental medwatch will be provided after investigation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8010042-2013-00219
MDR Report Key3574064
Report Source01,05,06,07
Date Received2013-11-04
Date of Report2013-10-10
Date of Event2013-10-09
Date Facility Aware2013-11-04
Report Date2013-11-04
Date Mfgr Received2013-10-10
Date Added to Maude2014-02-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJANICE PEVIDE
Manufacturer Street45 BARBOUR POND DRIVE
Manufacturer CityWAYNE NJ 07470
Manufacturer CountryUS
Manufacturer Postal07470
Manufacturer Phone9737097753
Manufacturer G1MAQUET CRITICAL CARE AB
Manufacturer Street2 ROENTGENVAGEN
Manufacturer CitySOLNA
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSUPPORT ARM 177
Product CodeIOY
Date Received2013-11-04
Model NumberNA
Catalog Number6481720
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAQUET CRITICAL CARE AB
Manufacturer Address2 ROENTGENVAGEN SOLNA SW


Patients

Patient NumberTreatmentOutcomeDate
10 2013-11-04

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