SUPPORT ARM 6481720

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-03 for SUPPORT ARM 6481720 manufactured by Maquet Critical Care Ab.

Event Text Entries

[116058580] The damaged support arm was discarded, therefore it was not returned for our investigation. A picture of the broken arm was sent. The evaluation of the returned picture of the support arm shows a broken molded section area at the joint nearest to the bracket. However, the picture did not show the date stamp therefore the manufacturing date is unknown. The support arm is a casting and it most probably developed a crack at an earlier occasion either by overloading or impact and this led to the reported breaking. Previous investigations of the support arm led to a change of the manufacturing process in order to obtain a higher mechanical strength of the support arm. This change was implemented in production during may 2009. (b)(4). (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[116058581] It was reported that the support arm was damaged. There was no patient involvement. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010042-2018-00404
MDR Report Key7747249
Date Received2018-08-03
Date of Report2018-08-27
Date of Event2018-07-17
Date Mfgr Received2018-07-17
Date Added to Maude2018-08-03
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 StreetMAQUET CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Manufacturer G1MAGNUS LINDQVIST
Manufacturer StreetMAQUET CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSUPPORT ARM
Generic NameSUPPORT, ARM
Product CodeIOY
Date Received2018-08-03
Catalog Number6481720
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAQUET CRITICAL CARE AB
Manufacturer AddressSOLNA SW


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-03

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