MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. DYNASTY A-CLASS 40MM STD GROUP F CROSSLINKED POL; HIP COMPONENT

Model Number DLXPGF40

Device Problem Detachment of Device or Device Component (2907)

Patient Problem Arthritis (1723)

Event Type  Injury  

Manufacturer Narrative

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

Event Description

Allegedly, patient was revised for liner disassociation.Time to revision was 57 months component not revised: dynasty(r) shell product id: dxxxgf56 lot id: not indicated.Additional information : indication for surgery was osteoarthritis.Bmi: 33.

• Brand Name: DYNASTY A-CLASS 40MM STD GROUP F CROSSLINKED POL
• 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: 10311825
• MDR Text Key: 199981889
• Report Number: 3010536692-2020-00498
• Device Sequence Number: 1
• Product Code: JDI
• UDI-Device Identifier: M684DLXPGF401
• UDI-Public: M684DLXPGF401
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K061547
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: other,study
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 10/28/2020

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
• Device Operator: Other
• Device Model Number: DLXPGF40
• Device Catalogue Number: DLXPGF40
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 07/01/2020
• Initial Date Manufacturer Received: 07/01/2020
• Initial Date FDA Received: 07/22/2020
• Supplement Dates Manufacturer Received: 07/01/2020
• Supplement Dates FDA Received: 10/28/2020
• 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
• Patient Age: 70 YR