PROSTHESIS, ELBOW, HEMI-, RADIAL - STEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-01-28 for PROSTHESIS, ELBOW, HEMI-, RADIAL - STEM manufactured by Acumedllc.

Event Text Entries

[183718147] Additional mdrs associated with this event: 3025141-2020-00022: head, 3025141-2020-00023: neck.
Patient Sequence No: 1, Text Type: N, H10


[183718148] Patient received a arh slide loc radial head replacement system in 2017. X-ray shows that the head/neck construct appears to be dissociated from the stem. Revision surgery has not been scheduled to date.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3025141-2020-00024
MDR Report Key9637596
Report SourceDISTRIBUTOR
Date Received2020-01-28
Date of Report2020-01-21
Date Mfgr Received2020-01-21
Date Added to Maude2020-01-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. MICKI ANDERSON
Manufacturer Street5885 NE CORNELIUS PASS ROAD
Manufacturer CityHILLSBORO OR 97124
Manufacturer CountryUS
Manufacturer Postal97124
Manufacturer G1ACUMEDLLC
Manufacturer Street5885 NE CORNELIUS PASS ROAD
Manufacturer CityHILLSBORO OR 97124
Manufacturer CountryUS
Manufacturer Postal Code97124
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NamePROSTHESIS, ELBOW, HEMI-, RADIAL - STEM
Product CodeKWI
Date Received2020-01-28
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerACUMEDLLC
Manufacturer Address5885 NE CORNELIUS PASS ROAD HILLSBORO OR 97124 US 97124


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-28

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