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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. CONSERVE PLUS CUP; HIP COMPONENT

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MICROPORT ORTHOPEDICS INC. CONSERVE PLUS CUP; HIP COMPONENT Back to Search Results
Model Number 38025460
Device Problems Unstable (1667); Failure to Osseointegrate (1863)
Patient Problem Hematoma (1884)
Event Type  Injury  
Manufacturer Narrative
Investigation completed.Evaluation codes added.
 
Event Description
Allegedly, the patient's acetabular components were revised on (b)(6) 2008 due to rotational instability, and a hematoma was found and removed during the operation.This patient was later revised on (b)(6) 2017 due to a fractured modular neck (incident group (b)(4)).
 
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Brand Name
CONSERVE PLUS CUP
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 Key10502566
MDR Text Key205946550
Report Number3010536692-2020-00605
Device Sequence Number1
Product Code KWA
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type other
Reporter Occupation Physician
Type of Report Initial
Report Date 09/07/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/08/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model Number38025460
Device Catalogue Number38025460
Device Lot Number087459174
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date08/19/2020
Date Manufacturer Received08/19/2020
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
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