AXOR II 1288

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-10-01 for AXOR II 1288 manufactured by Integrum Ab.

Event Text Entries

[122309849] Unwanted release of prosthesis when walking. Patient describes device loosening while walking. No harm to patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011386779-2018-00011
MDR Report Key7923296
Report SourceHEALTH PROFESSIONAL
Date Received2018-10-01
Date of Report2018-11-07
Date of Event2018-08-21
Date Facility Aware2018-08-21
Report Date2018-08-21
Date Reported to Mfgr2018-08-21
Date Mfgr Received2018-08-21
Device Manufacturer Date2017-05-22
Date Added to Maude2018-10-01
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 ContactMR. NIKLAS HOFVERBERG
Manufacturer StreetKROKSL
Manufacturer CityM
Manufacturer G1INTEGRUM AB
Manufacturer StreetKROKSLATTS FABRIKER 50
Manufacturer CityM 43137
Manufacturer CountrySW
Manufacturer Postal Code43137
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAXOR II
Generic NameAXOR II
Product CodePJY
Date Received2018-10-01
Returned To Mfg2018-08-21
Model Number1288
Catalog Number1288
Lot NumberU-86792-16
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Age16 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerINTEGRUM AB
Manufacturer AddressKROKSL?TTS FABRIKER 50 M?LNDAL, M?LNDAL 43137 SW 43137


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-10-01

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