MAUDE Adverse Event Report: ARTHREX, INC. HUMERAL INSERT XS 33+3MM CONSTRAINED; SHOULDR PROSTH, REVERSE CONFIG

Model Number HUMERAL INSERT XS 33+3MM CONSTRAINED

Device Problem Inadequacy of Device Shape and/or Size (1583)

Patient Problem Insufficient Information (4580)

Event Date 02/21/2024

Event Type  malfunction  

Manufacturer Narrative

The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.Investigation is in process.A follow-up report will be provided upon availability of additional information.

Event Description

On 03/05/2024, it was reported by a sales representative via e-mail that an ar-9502f-33lcpc univers revers suture cup, ar-9503xs-03c humeral insert, and an ar-9501-05p univers revers¿ humeral stem failed in a case.This occurred during a revers total shoulder procedure on (b)(6) 2024 when the surgeon decided to change the poly size when trying to extract the implant.The rest of the construct became loose.They then had to exchange for a bigger stem, a new suture cup, and the correctly sized poly.

• Brand Name: HUMERAL INSERT XS 33+3MM CONSTRAINED
• Type of Device: SHOULDR PROSTH, REVERSE CONFIG
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer (Section G): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer Contact: jared engle ; 8009337001
• MDR Report Key: 18943693
• MDR Text Key: 338154967
• Report Number: 1220246-2024-01575
• Device Sequence Number: 1
• Product Code: HSD
• UDI-Device Identifier: 00888867406865
• UDI-Public: 00888867406865
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K221232
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Distributor
• Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial
• Report Date: 03/20/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: HUMERAL INSERT XS 33+3MM CONSTRAINED
• Device Catalogue Number: AR-9503XS-03C
• Device Lot Number: 23.00357
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 03/06/2024
• Initial Date FDA Received: 03/20/2024
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 05/01/2023
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1