MAUDE Adverse Event Report: ENCORE MEDICAL L.P RSP MONOBLOCK SOCKET INSERT, 32MM +4MM, SEMICONSTRAINED, HXE-PLUS; SHOULDER PROSTHESIS, REVERSE CONFIGURATION

Catalog Number	509-01-432
Medical Device Problem Code	No Apparent Adverse Event (3189)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	04/05/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - infection.
Additional Manufacturer Narrative
Complaint has been evaluated and is similar to previous report number 1644408-2022-01413; 509-01-432,s808 - infection ,revision surgery if additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.

• Brand Name: RSP MONOBLOCK SOCKET INSERT, 32MM +4MM, SEMICONSTRAINED, HXE-PLUS
• Common Device Name: SHOULDER PROSTHESIS, REVERSE CONFIGURATION
• Manufacturer (Section D): ENCORE MEDICAL L.P; 9800 metric blvd; austin TX 78758
• Manufacturer (Section G): ENCORE MEDICAL L.P; 9800 metric blvd; austin TX 78758
• Manufacturer Contact: james mcmahon ; 9800 metric blvd; austin, TX 78758
• MDR Report Key: 19244322
• Report Number: 1644408-2024-00620
• Device Sequence Number: 7495160
• Product Code: PHX
• UDI-Device Identifier: 00888912144650
• UDI-Public: 00888912144650
• Combination Product (Y/N): N
• Initial Reporter State: KS
• Initial Reporter Country: US
• PMA/510(K) Number: K051075
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2024
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/03/2024

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 Catalogue Number: 509-01-432
• Device Lot Number: 389P1216A
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/05/2024
• Initial Report FDA Received Date: 05/03/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/14/2023
• 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: 506-03-114 LOT: 831C2426; 506-03-118 LOT: 832C2108; 506-03-126 LOT: 834C2223; 506-03-126 LOT: 834C2231; 508-32-101 LOT: 862C4192; 508-32-204 LOT: 769P2501; 530-08-048 LOT: 1484A1111
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 58 YR
• Patient Sex: Male