MAUDE Adverse Event Report: ARTHREX, INC. UNIVERS REVS CUP,39/NEUTAL CTD; SHOULDR PROSTH, REVERSE CONFIG

Model Number	UNIVERS REVS CUP,39/NEUTAL CTD
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	01/15/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that a patient underwent multiple surgeries on the reported shoulder prosthesis.It was further reported that some revision surgeries have been performed.It was further reported that the customer has in addition to the reported devices five screws (1 silver, 3 green, 1 purple), a base plate, glenosphere, a inlay and a post.
Additional Manufacturer Narrative
Investigation is in process.A follow-up report will be provided upon availability of additional information.
Additional Manufacturer Narrative
Complaint allegation is confirmed.One unpackaged ar-9502-39cpc univers revers cup - cap coated 39 / neutral batch number: 23.01149 was received for investigation.Visual evaluation noted the hex of the screw was damaged.The most likely cause for this can be attributed to misuse due to excessive force being applied while being extracted.Functional testing was performed by assembling the returned device with the returned mating devices.No issues were noted when the devices were assembled together.The most likely cause for the reported failure can be attributed to a patient-specific event.

• Brand Name: UNIVERS REVS CUP,39/NEUTAL CTD
• Common Device Name: 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: 21323148
• Report Number: 1220246-2025-00267
• Device Sequence Number: 12741978
• Product Code: PHX
• UDI-Device Identifier: 00888867061156
• UDI-Public: 00888867061156
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K142863
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup
• Report Date (Section B): 04/09/2025

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 Model Number: UNIVERS REVS CUP,39/NEUTAL CTD
• Device Catalogue Number: AR-9502-39CPC
• Device Lot Number: 23.01149
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/15/2025
• Supplement Date Received by Manufacturer: 03/27/2025
• Initial Report FDA Received Date: 02/06/2025
• Supplement Report FDA Received Date: 04/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown