MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. CONSERVE BFH HEAD 42MM MEDIUM NECK; HIP COMPONENT

Model Number	38014200
Medical Device Problem Codes	Corroded (1131); Material Disintegration (1177)
Health Effect - Clinical Code	Metal Related Pathology (4530)
Type of Reportable Event	Serious Injury
Event or Problem Description
Allegedly, the patient was revised due to metal debris, corrosion and resultant metal ions due to the metal-on-metal design between the articulating surfaces.

• Brand Name: CONSERVE BFH HEAD 42MM MEDIUM NECK
• Common Device Name: HIP COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• MDR Report Key: 11268519
• Report Number: 3010536692-2021-00052
• Device Sequence Number: 4068822
• Product Code: KWA
• UDI-Device Identifier: M684380142001
• UDI-Public: M684380142001
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K021349
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2003
• Device Explanted Year: 2019
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: other
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 02/02/2021

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 Model Number: 38014200
• Device Catalogue Number: 38014200
• Device Lot Number: 08351687
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 01/12/2021
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/12/2021
• Initial Report FDA Received Date: 02/02/2021
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention