MAUDE Adverse Event Report: ENCORE MEDICAL L.P. DJO SURGICAL; LINER, ACETABULAR, HOODED, NEUTRAL, 10°, HXL/FMP, 36MM ID, MP7

Catalog Number	932-36-252
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Implant Pain (4561)
Date of Event	08/07/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Additional reporting on this event will be provided as a supplemental report to this document as soon as it becomes available.
Event or Problem Description
Revision surgery - due to patient presented with hip pain.Surgeon elected to do a head and liner swap out.
Additional Manufacturer Narrative
Complaint has been evaluated and is similar to: (b)(4); 932-36-752, s807 - pain, revision surgery note: the primary or previous dticket was not provided, therefore, the items revised could not be verified.If additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.

• Brand Name: DJO SURGICAL
• Common Device Name: LINER, ACETABULAR, HOODED, NEUTRAL, 10°, HXL/FMP, 36MM ID, MP7
• 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: stacey bonnell ; 9800 metric blvd; austin, TX 78758
• MDR Report Key: 20131615
• Report Number: 1644408-2024-01372
• Device Sequence Number: 17947407
• Product Code: LPH
• UDI-Device Identifier: 00888912100076
• UDI-Public: 00888912100076
• Combination Product (Y/N): N
• Initial Reporter State: RI
• Initial Reporter Country: US
• PMA/510(K) Number: K130365
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2024
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/31/2024

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 Expiration Date: 06/28/2017
• Device Catalogue Number: 932-36-252
• Device Lot Number: 728F1058
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/07/2024
• Supplement Date Received by Manufacturer: 10/03/2024
• Initial Report FDA Received Date: 09/03/2024
• Supplement Report FDA Received Date: 10/31/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/18/2012
• 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: 497-36-000 LOT: 638C1048; 932-36-252 LOT: 728F1058
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown