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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ENCORE MEDICAL L.P. MOVATION KNEE MOVATION TIBIAL INSERT, SIZE 8, 9MM VE

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ENCORE MEDICAL L.P. MOVATION KNEE MOVATION TIBIAL INSERT, SIZE 8, 9MM VE Back to Search Results
Model Number 292-09-708
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Unspecified Infection (1930)
Event Date 06/14/2017
Event Type  Injury  
Manufacturer Narrative
The reason for this revision surgery was reported as an infection. The previous surgery and the revision detailed in this investigation occurred 50 days apart. No information was submitted with the complaint regarding pre-existing conditions of the patient or any activities the patient was involved in that may have contributed to the infection or inhibited the patient's immune system. The healthcare professional indicated there was no delay in surgery and another suitable device was available for use. The revision surgery was completed as intended. The device was disposed of at the hospital and not made available to djo surgical for examination. A review of the implant device history records (dhrs) show that the reported component used in the previous surgery met design and manufacturing requirements. There were no non-conforming material reports (ncmrs) associated with the product that may have contributed to an infection. Customer complaint history of the reported device showed no present trends or on-going issues that are in need of review. The device was verified to have gone through an acceptable sterilization process and was within it's expiration date at the time of use during the previous surgery. The root cause of this complaint was a revision surgery due to an infection. There were no findings during this investigation that indicate that the reported device was the root cause or had a direct connection with the patient's infection. There are multiple factors that may contribute to an infection that are outside of the control of djo surgical. There are no indications of a product or process issue affecting implant safety or effectiveness. Inventory containment is not required as there are no indications of a product or process issue affecting implant safety or effectiveness. The revision surgery was completed successfully.
 
Event Description
Revision surgery - due to the patient having an infection and an irrigation & drainage (i&d) procedure. The surgeon swapped the poly. No problem with original implant.
 
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Brand NameMOVATION KNEE
Type of DeviceMOVATION TIBIAL INSERT, SIZE 8, 9MM VE
Manufacturer (Section D)
ENCORE MEDICAL L.P.
9800 metric blvd.
austin TX 78758 5445
Manufacturer (Section G)
ENCORE MEDICAL L.P.
9800 metric blvd.
austin TX 78758 5445
Manufacturer Contact
teffany hutto
9800 metric blvd.
austin, TX 78758-5445
MDR Report Key6712462
MDR Text Key151864441
Report Number1644408-2017-00618
Device Sequence Number1
Product Code OIY
UDI-Device Identifier00888912112437
UDI-Public(01)00888912112437
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K121727
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Reporter Occupation
Type of Report Initial,Followup
Report Date 08/17/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/13/2017
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Device Expiration Date10/28/2019
Device Model Number292-09-708
Device Catalogue Number292-09-708
Device Lot Number328N1007
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? No
Event Location No Information
Date Manufacturer Received07/19/2017
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured10/16/2014
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient Treatment Data
Date Received: 07/13/2017 Patient Sequence Number: 1
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