MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. CONSERVE® TOTAL 38MM BCH® FEMORAL HEAD; HIP COMPONENT

Model Number	38CH3800
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Insufficient Information (4580)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This event will be updated once the investigation is complete.Trends will be evaluated.
Event or Problem Description
Allegedly, components revised for unknown reasons.High mbi.
Additional Manufacturer Narrative
Due to additional information received and after further analysis of this event , the device involved in this manufacturer reference report (b)(4) has been classified as "no complaint stated" since there is no alleged deficiency against the device.Please void this report.
Additional Manufacturer Narrative
Previous report had a minor human error in this description.Please read correctly below: due to additional information received and after further analysis of this event , the device involved in this manufacturer reference report has been classified as "no complaint stated" since there is no alleged deficiency against the device.Please void this report.

• Brand Name: CONSERVE® TOTAL 38MM BCH® FEMORAL HEAD
• 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: 13397179
• Report Number: 3010536692-2022-00028
• Device Sequence Number: 4950706
• Product Code: LZO
• UDI-Device Identifier: M68438CH38001
• UDI-Public: M68438CH38001
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K072656
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 07/06/2022

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: 38CH3800
• Device Catalogue Number: 38CH3800
• Device Lot Number: 1479667
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 01/10/2022
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/10/2022
• Supplement Date Received by Manufacturer: 01/10/2022; 01/10/2022; 01/10/2022
• Initial Report FDA Received Date: 01/31/2022
• Supplement Report FDA Received Date: 03/18/2022; 07/06/2022; 07/06/2022
• 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 Age: 53 YR
• Patient Sex: Female