MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. PROFEMUR® PRESERVE STEM SIZE 5; HIP COMPONENT

Model Number	PRPR0005
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	02/17/2016
Type of Reportable Event	Serious Injury
Event or Problem Description
Allegedly, on report: (b)(4) it is mentioned that the patient had a preserve stem implanted but then the x-ray control showed femur fracture proximal and the component was revised.The preserve stem isn't part of the clinical study (b)(6) and it's mentioned that a gladiator stem that is part of the study was implanted after the revision of the preserve stem.
Additional Manufacturer Narrative
This event will be updated once the investigation is complete.Trends will be evaluated.

• Brand Name: PROFEMUR® PRESERVE STEM SIZE 5
• Common Device Name: HIP COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer (Section G): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer Contact: 5677 airline road; arlington, TN 38002 ; 9018674771
• MDR Report Key: 12714251
• Report Number: 3010536692-2021-00548
• Device Sequence Number: 4027765
• Product Code: JDL
• UDI-Device Identifier: M684PRPR00051
• UDI-Public: M684PRPR00051
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K112080
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 01/31/2022

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: Other
• Device Model Number: PRPR0005
• Device Catalogue Number: PRPR0005
• Device Lot Number: 1595705
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 10/11/2021
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/11/2021
• Supplement Date Received by Manufacturer: 10/11/2021
• Initial Report FDA Received Date: 10/28/2021
• Supplement Report FDA Received Date: 01/31/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown