MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. PROFEMUR(R) GLADIATOR(R) STEM; HIP COMPONENT

Model Number PRGL-CM06

Device Problem Device Dislodged or Dislocated (2923)

Patient Problem No Information (3190)

Event Date 08/14/2014

Event Type  Injury  

Manufacturer Narrative

This complaint will be updated once the investigation is complete.Trends will be evaluated.

Event Description

After intervention, patient continued with discomfort in the right hip.Patient was seen in the clinic in (b)(6) and had been during stretches with a therapist.An x-ray revealed he has a dislocated hip.He was admitted for a hip revision.Dynasty® biofoam shell, dynasty® a-class® poly liner, profemur® plus cocr modular neck, conserve® a-class® bfh head, and screw were revised (right).Sade # (b)(4).

• Brand Name: PROFEMUR(R) GLADIATOR(R) STEM
• Type of Device: 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: 8392208
• MDR Text Key: 137880544
• Report Number: 3010536692-2019-00488
• Device Sequence Number: 1
• Product Code: JDL
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 03/05/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/05/2019
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Other
• Device Model Number: PRGL-CM06
• Device Catalogue Number: PRGL-CM06
• Device Lot Number: 1483890
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 02/20/2019
• Date Manufacturer Received: 02/20/2019
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention