HUMELOCK II 313-0706

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-13 for HUMELOCK II 313-0706 manufactured by Fx Solutions.

Event Text Entries

[188258032] Revision surgery on (b)(6) 2019 for dislocation approximately three weeks after primary surgery. Surgeon explanted 135/145 36/+6 humeral cup and replaced it with both a 36/+3 humeral cup and a 135/145 reversed adapter for an extra +9mm, for a total spacing of +12mm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009532798-2020-00032
MDR Report Key9829484
Report SourceOTHER
Date Received2020-03-13
Date of Report2020-02-27
Date of Event2019-12-13
Date Mfgr Received2020-01-20
Device Manufacturer Date2018-10-31
Date Added to Maude2020-03-13
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 ContactMR. CEDRIC JOLY
Manufacturer Street1663 RUE DE MAJORNAS
Manufacturer CityVIRIAT, 01440
Manufacturer CountryFR
Manufacturer Postal01440
Manufacturer G1FX SOLUTIONS
Manufacturer Street1663 RUE DE MAJORNAS
Manufacturer CityVIRIAT, 01440
Manufacturer CountryFR
Manufacturer Postal Code01440
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUMELOCK II
Generic NameSHOULDER PROTHESIS
Product CodeHSD
Date Received2020-03-13
Catalog Number313-0706
Lot NumberL2882
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerFX SOLUTIONS
Manufacturer Address1663 RUE DE MAJORNAS VIRIAT, 01440 FR 01440


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-13

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