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ENCORE MEDICAL L.P. 3D KNEE INSERT, 3D EX SZ 10LT 9MM Back to Search Results
Model Number 391-09-710
Device Problem Insufficient Information (3190)
Patient Problem Unspecified Infection (1930)
Event Date 02/21/2018
Event Type  Injury  
Event Description
Revision surgery - due to the patient having an infection.
Manufacturer Narrative
The reason for this revision surgery was due to an infection. The previous surgery and the revision detailed in this investigation occurred 2. 2 years 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. 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.
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Brand Name3D KNEE
Type of DeviceINSERT, 3D EX SZ 10LT 9MM
Manufacturer (Section D)
9800 metric blvd
austin TX 78758 5445
MDR Report Key7314727
MDR Text Key101562085
Report Number1644408-2018-00176
Device Sequence Number1
Product Code OIY
UDI-Device Identifier00888912118996
Combination Product (y/n)N
PMA/PMN Number
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Type of Report Initial,Followup
Report Date 03/12/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/05/2018
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Device Expiration Date07/28/2019
Device Model Number391-09-710
Device Catalogue Number391-09-710
Device Lot Number59605091
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Event Location No Information
Date Manufacturer Received03/12/2018
Is This a Reprocessed and Reused Single-Use Device? No

Patient Treatment Data
Date Received: 03/05/2018 Patient Sequence Number: 1