MAUDE Adverse Event Report: FX SHOULDER SOLUTIONS DALLAS HUMELOCK REVERSED; REVERSE SHOULDER PROSTHESIS

Catalog Number	105-3610
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Inadequate Osseointegration (2646)
Date of Event	01/03/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision occurred approximately 4 years after the primary surgery, which occurred on (b)(6) 2021.No fall or other trauma reported.Revision occurred due to loosening of glenoid components.36 mm centered glenosphere and 36 mm + 3 standard humeral cup were explanted.These parts were replaced with a 36 mm + 3 centered glenosphere and a 36 mm + 6 standard humeral cup.Revision occurred approximately 4 years after the primary surgery, which occurred on (b)(6) 2021.No fall or other trauma reported.Revision occurred due to loosening of glenoid components.36 mm centered glenosphere and 36 mm + 3 standard humeral cup were explanted.These parts were replaced with a 36 mm + 3 centered glenosphere and a 36 mm + 6 standard humeral cup.
Additional Manufacturer Narrative
Revision occurred after 4 years due to loosening of glenoid components.No actual, implied, or suspect link to fx product.

• Brand Name: HUMELOCK REVERSED
• Common Device Name: REVERSE SHOULDER PROSTHESIS
• Manufacturer (Section D): FX SHOULDER SOLUTIONS DALLAS; 15920 addison road; addison TX 75001
• Manufacturer (Section G): FX SHOULDER SOLUTIONS DALLAS; 15920 addison road; addison TX 75001
• Manufacturer Contact: tristan mahler ; 15920 addison road; addison, TX 75001 ; 7137326920
• MDR Report Key: 21267658
• Report Number: 3014128390-2025-00006
• Device Sequence Number: 17054379
• Product Code: PHX
• UDI-Device Identifier: 03701037300268
• UDI-Public: 03701037300268
• Combination Product (Y/N): N
• Initial Reporter State: MD
• Initial Reporter Country: US
• PMA/510(K) Number: K150488
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 01/03/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 09/01/2025
• Device Catalogue Number: 105-3610
• Device Lot Number: P0653
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/03/2025
• Initial Report FDA Received Date: 01/29/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 09/01/2020
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: PART: 103-0803 LOT: N0194
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Sex: Unknown