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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. EVOLUTION® MP? CS INSERT SIZE 5 STANDARD 12MM RIGH; KNEE COMPONENT

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MICROPORT ORTHOPEDICS INC. EVOLUTION® MP? CS INSERT SIZE 5 STANDARD 12MM RIGH; KNEE COMPONENT Back to Search Results
Model Number EIS5S12R
Device Problem Unstable (1667)
Patient Problem Pain (1994)
Event Type  Injury  
Event Description
Allegedly, patient underwent bilateral tkr on (b)(6) 2020, revised on (b)(6) 2023.Patient presented with instability on the lateral side and surgeon also felt that replacing the patella might eliminate the anterior knee pain they were experiencing.Patella added and 12mm insert replaced with a 14mm one.Australia: (b)(4).
 
Manufacturer Narrative
This event will be updated once the investigation is complete.Trends will be evaluated.
 
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Brand Name
EVOLUTION® MP? CS INSERT SIZE 5 STANDARD 12MM RIGH
Type of Device
KNEE COMPONENT
Manufacturer (Section D)
MICROPORT ORTHOPEDICS INC.
5677 airline rd.
arlington TN 38002
Manufacturer Contact
rachael wise
5677 airline road
arlington, TN 38002
9018674771
MDR Report Key17894119
MDR Text Key325342705
Report Number3010536692-2023-00176
Device Sequence Number1
Product Code HRY
UDI-Device IdentifierM684EIS5S12R1
UDI-PublicM684EIS5S12R1
Combination Product (y/n)N
Reporter Country CodeAS
PMA/PMN Number
K093552
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Distributor
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 12/12/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/09/2023
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Model NumberEIS5S12R
Device Catalogue NumberEIS5S12R
Device Lot Number1767648
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Date Manufacturer Received09/13/2023
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age64 YR
Patient SexFemale
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