FDA Adverse Event Injury Summary report: N

HUMELOCK REVERSED

MDR report key: 12096030 · Received June 30, 2021

Report

Report Number
3014128390-2021-00035
Event Type
Injury
Date Received
June 30, 2021
Date of Event
June 3, 2021
Report Date
June 30, 2021
Manufacturer
FX SOLUTIONS SAS
Product Code
PHX
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PATIENT REVISED ON (B)(6) 2021 DUE TO DISLOCATION FROM FALLING OUT OF BED, APPROXIMATELY 6 WEEKS AFTER PRIMARY SURGERY. SURGEON EXPLANTED 36/+9 STANDARD HUMERAL CUP AND REPLACED IT WITH A 36/+6 STABILITY HUMERAL CUP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
989198 HUMELOCK REVERSED REVERSED SHOULDER PROSTHESIS PHX FX SOLUTIONS SAS N1431

Patients

Seq Age Sex Outcome Treatment
1 63 YR Hospitalization| R