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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ENCORE MEDICAL L.P. X-ALT HIP; LINER 10 DEG HOODED-NEU, MP10, HXE-PLUS, 44MM

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ENCORE MEDICAL L.P. X-ALT HIP; LINER 10 DEG HOODED-NEU, MP10, HXE-PLUS, 44MM Back to Search Results
Model Number 932-44-760
Health Effect - Clinical Code Unspecified Infection (1930)
Date of Event 08/25/2020
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
The reason for this revision surgery was reported as an infection.The previous surgery and the surgery detailed in this event occurred 1.5 years apart.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 devices were disposed of at hospital and not made available to djo surgical for examination.A review of the device history records (dhr) show that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements.There were no non-conforming material reports (ncmr) associated with the products that may have contributed to the reported event.The devices were verified to have gone through an acceptable sterilization process and were within its expiration date at the time of the previous surgery.Customer complaint history of the reported devices showed no present trends or on-going issues that are needing a review.The root cause of this complaint was a revision surgery due to an infection.There were no findings during this evaluation that indicate the reported devices were the source or had a direct connection with the patient's infection.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.There are multiple factors that may contribute to an infection that are outside the control of djo surgical.There are no indications of a product or process issue affecting implant safety or effectiveness.Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.
 
Event or Problem Description
Revision surgery - the patient presented with signs of infection, the surgeon went intending to wash out and debride and ultimately decided to remove components so the infection could reside and he would revise the hip at a later date.
 
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Brand Name
X-ALT HIP
Common Device Name
LINER 10 DEG HOODED-NEU, MP10, HXE-PLUS, 44MM
Manufacturer (Section D)
ENCORE MEDICAL L.P.
9800 metric blvd
austin, tx 78758-5445
MDR Report Key10568409
Report Number1644408-2020-00804
Device Sequence Number2670674
Product Code OQG
UDI-Device Identifier00888912100472
UDI-Public(01)00888912100472
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K130365
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2019
Device Explanted Year2020
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source company representative
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 09/22/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Expiration Date10/10/2022
Device Model Number932-44-760
Device Catalogue Number932-44-760
Device Lot Number816N1944
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/25/2020
Initial Report FDA Received Date09/22/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Concomitant Medical Products
and Therapy/Usage Dates
010-55-015 LOT 003A1195; 010-55-015 LOT 003A1205; 010-55-020 LOT 005A1266; 010-55-020 LOT 005A1277; 010-55-025 LOT 006A1404; 010-55-025 LOT 006A1418; 400-04-440 LOT 885B1011; 400-05-000 LOT 886B1072; 430-93-060 LOT 046H1018
Outcome Attributed to Adverse Event Required Intervention;
Patient Age54 YR
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