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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. RIM-LOCK BIOLOX DELTA CERAMIC LINER; HIP COMPONENT

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MICROPORT ORTHOPEDICS INC. RIM-LOCK BIOLOX DELTA CERAMIC LINER; HIP COMPONENT Back to Search Results
Model Number PHA0-4510
Device Problem Break (1069)
Patient Problem No Information (3190)
Event Type  Injury  
Manufacturer Narrative
This complaint will be updated once the investigation is complete.Trends will be evaluated.
 
Event Description
Allegedly a little shard came off of the rim of the liner.Surgeon is an experienced procotyl l user and both surgeon as sales rep are 100% sure that cups was correctly positioned.See enclosed x ray pictures.
 
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Brand Name
RIM-LOCK BIOLOX DELTA CERAMIC LINER
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 Key8443324
MDR Text Key139543727
Report Number3010536692-2019-00555
Device Sequence Number1
Product Code LZO
Combination Product (y/n)N
Reporter Country CodeBE
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 03/20/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/22/2019
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Model NumberPHA0-4510
Device Catalogue NumberPHA0-4510
Device Lot Number1618247
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date03/11/2019
Date Manufacturer Received03/11/2019
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 Age49 YR
Patient Weight99
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