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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. EVOLUTION(TM) MP CS INSERT; KNEE COMPONENT

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MICROPORT ORTHOPEDICS INC. EVOLUTION(TM) MP CS INSERT; KNEE COMPONENT Back to Search Results
Model Number EIS7-S12R
Device Problem Insufficient Information (3190)
Patient Problem Neck Stiffness (2434)
Event Type  Injury  
Manufacturer Narrative
This complaint will be updated once the investigation is complete.Trends will be evaluated.
 
Event Description
Patient underwent right tkr on (b)(6) 2018, revised on (b)(6) 2019 due to stiffness.Poly liner revised with another of the same size.Liner had to be removed to access posterior knee, surgeon's decision was to replace liner rather than keeping the existing one.
 
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Brand Name
EVOLUTION(TM) MP CS INSERT
Type of Device
KNEE 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 Key8493581
MDR Text Key141300769
Report Number3010536692-2019-00618
Device Sequence Number1
Product Code HRY
Combination Product (y/n)N
Reporter Country CodeAU
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional
Reporter Occupation Physician
Type of Report Initial,Followup
Report Date 04/08/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/08/2019
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Model NumberEIS7-S12R
Device Catalogue NumberEIS7-S12R
Device Lot Number1687643
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date03/28/2019
Date Manufacturer Received03/28/2019
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;
Patient Age57 YR
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