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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD; HIP COMPONENT

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MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD; HIP COMPONENT Back to Search Results
Catalog Number 2600-0027
Device Problem Loose or Intermittent Connection (1371)
Patient Problem No Information (3190)
Event Type  Injury  
Manufacturer Narrative
This complaint will be updated once investigation is complete.Trends will be evaluated.
 
Event Description
Allegedly, patient was revised due aseptic loosening stem; other indication for revision (left).Sr njr number: (b)(4).First revision asa: p2 - mild disease not incapacitating.
 
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Brand Name
LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD
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 Key6898646
MDR Text Key87584033
Report Number3010536692-2017-01268
Device Sequence Number1
Product Code JDL
Combination Product (y/n)N
Reporter Country CodeGB
PMA/PMN Number
K004043
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional
Reporter Occupation Other
Type of Report Initial,Followup
Report Date 09/18/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/27/2017
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Catalogue Number2600-0027
Device Lot Number1430352
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Distributor Facility Aware Date09/18/2017
Date Manufacturer Received09/18/2017
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 Age68 YR
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