HUMELOCK REVERSED 312-3612

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 2020-03-20 for HUMELOCK REVERSED 312-3612 manufactured by Fx Solutions.

Event Text Entries

[184257147] The event took place outside of the united states (in (b)(6)) and was associated with a product that is also cleared for the market within the united states.
Patient Sequence No: 1, Text Type: N, H10


[184257148] Revision surgery due to an infection occurred (b)(6) 2019. The? 36/12 humeral stem,? 36/+3 humeral cup,? 36 glenosphere, glenoid baseplate and associated screws were removed and replaced by the? 36/14 humeral stem,? 36/+9 humeral cup,? 36 glenosphere, glenoid baseplate and associated screws. Primary surgery occurred (b)(6) 2016.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009532798-2020-19225
MDR Report Key9859060
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2019-04-18
Date Mfgr Received2019-04-19
Device Manufacturer Date2016-01-29
Date Added to Maude2020-03-20
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 REVERSED
Generic NameREVERSED SHOULDER PROTHESIS
Product CodePHX
Date Received2020-03-20
Catalog Number312-3612
Lot NumberJ768
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 2020-03-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.